CFTR mutations in three Latin American countries

We analyzed 192 cystic fibrosis (CF) alleles in three Latin American countries: Mexico, Colombia, and Venezuela. Mutation screening was performed by polymerase chain reaction (PCR) and a reverse dot blot detection kit that enables determination of 16 of the most common CF mutations worldwide. Mutati...

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Autores:
Tipo de recurso:
Fecha de publicación:
2000
Institución:
Universidad del Rosario
Repositorio:
Repositorio EdocUR - U. Rosario
Idioma:
eng
OAI Identifier:
oai:repository.urosario.edu.co:10336/25139
Acceso en línea:
https://doi.org/10.1002/(SICI)1096-8628(20000410)91:4<277::AID-AJMG7>3.0.CO;2-A
https://repository.urosario.edu.co/handle/10336/25139
Palabra clave:
Transmembrane conductance regulator
Article
Colombia
Cystic fibrosis
Disease association
Gene frequency
Gene mutation
Human
Major clinical study
Mexico
Priority journal
Venezuela
Colombia
Cystic fibrosis
Cystic fibrosis transmembrane conductance regulator
Gene frequency
Humans
Mexico
Mutation
Prevalence
Spain
Venezuela
Allele/mutation frequencies
Cystic fibrosis
Ethnic groups
Latin america
Rights
License
Bloqueado (Texto referencial)
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oai_identifier_str oai:repository.urosario.edu.co:10336/25139
network_acronym_str EDOCUR2
network_name_str Repositorio EdocUR - U. Rosario
repository_id_str
spelling 193318196005d8ae651-3bca-4393-91f3-090fb7a3af17441fc5e2-63cc-48dd-9c39-55657eabd689e0d200a4-92cf-4c7e-abd1-540c33649609a4ed220a-4fbb-4940-8f23-624d8c110a2dc8ab4e26-c1e0-4ab3-b6f0-45b720fac7b713116bb7-057a-444f-870a-e2f29ccd0830a3cfb896-9f76-41ee-9117-f36981ffc8074e2edd06-9f40-45b9-b3f7-27f92c8e24e6a7e021d1-0223-42c0-9e58-31404aaf707c873bc635-f24d-40eb-a5e5-da348c4c56d12020-06-11T13:22:29Z2020-06-11T13:22:29Z2000We analyzed 192 cystic fibrosis (CF) alleles in three Latin American countries: Mexico, Colombia, and Venezuela. Mutation screening was performed by polymerase chain reaction (PCR) and a reverse dot blot detection kit that enables determination of 16 of the most common CF mutations worldwide. Mutations were detected in 47.9% of the screened CF alleles. The most prevalent CF allele was ?F508 (39.6%). The remaining 16 non-?F508 detectable mutations represented 8.3% of the CF alleles. Among them, the G542X, N1303K, and 3849+10kb C > T were the most common. Although the frequency of ?F508 described here is lower than that reported for Caucasian populations, including in Spain, it is remarkable that mutation prevalences found in this study resemble those observed in Spain. Two of these mutations, G542X and 3849+10kb C>T, that were relevant in this analysis, have a particularly high incidence in Spanish communities. The low frequency of ?F508 described here may be explained by the Amerindian, Caucasian, and Black admixture that occurred in Latin America after the discovery of the New World, and also by the probable occurrence of mutations contributed by the original natives, which were undetectable in this analysis. (C) 2000 Wiley- Liss, Inc.application/pdfhttps://doi.org/10.1002/(SICI)1096-8628(20000410)91:4<277::AID-AJMG7>3.0.CO;2-Ahttps://repository.urosario.edu.co/handle/10336/25139engAmerican Journal of Medical Genetics279No. 4277American Journal of Medical GeneticsVol. 91American Journal of Medical Genetics, ISSN:, Vol.91, No.4 (2000); pp. 277-279https://onlinelibrary.wiley.com/doi/abs/10.1002/%28SICI%291096-8628%2820000410%2991%3A4%3C277%3A%3AAID-AJMG7%3E3.0.CO%3B2-ABloqueado (Texto referencial)http://purl.org/coar/access_right/c_14cbinstname:Universidad del Rosarioreponame:Repositorio Institucional EdocURTransmembrane conductance regulatorArticleColombiaCystic fibrosisDisease associationGene frequencyGene mutationHumanMajor clinical studyMexicoPriority journalVenezuelaColombiaCystic fibrosisCystic fibrosis transmembrane conductance regulatorGene frequencyHumansMexicoMutationPrevalenceSpainVenezuelaAllele/mutation frequenciesCystic fibrosisEthnic groupsLatin americaCFTR mutations in three Latin American countriesarticleArtículohttp://purl.org/coar/version/c_970fb48d4fbd8a85http://purl.org/coar/resource_type/c_6501Restrepo Fernández, Carlos MartínPineda L.Rojas-Martínez A.Gutiérrez C.A.Morales A.Gómez Y.Villalobos M.C.Borjas L.Delgado W.Myers A.Barrera-Saldaña H.A.10336/25139oai:repository.urosario.edu.co:10336/251392021-10-07 16:35:40.109https://repository.urosario.edu.coRepositorio institucional EdocURedocur@urosario.edu.co
dc.title.spa.fl_str_mv CFTR mutations in three Latin American countries
title CFTR mutations in three Latin American countries
spellingShingle CFTR mutations in three Latin American countries
Transmembrane conductance regulator
Article
Colombia
Cystic fibrosis
Disease association
Gene frequency
Gene mutation
Human
Major clinical study
Mexico
Priority journal
Venezuela
Colombia
Cystic fibrosis
Cystic fibrosis transmembrane conductance regulator
Gene frequency
Humans
Mexico
Mutation
Prevalence
Spain
Venezuela
Allele/mutation frequencies
Cystic fibrosis
Ethnic groups
Latin america
title_short CFTR mutations in three Latin American countries
title_full CFTR mutations in three Latin American countries
title_fullStr CFTR mutations in three Latin American countries
title_full_unstemmed CFTR mutations in three Latin American countries
title_sort CFTR mutations in three Latin American countries
dc.subject.keyword.spa.fl_str_mv Transmembrane conductance regulator
Article
Colombia
Cystic fibrosis
Disease association
Gene frequency
Gene mutation
Human
Major clinical study
Mexico
Priority journal
Venezuela
Colombia
Cystic fibrosis
Cystic fibrosis transmembrane conductance regulator
Gene frequency
Humans
Mexico
Mutation
Prevalence
Spain
Venezuela
Allele/mutation frequencies
Cystic fibrosis
Ethnic groups
Latin america
topic Transmembrane conductance regulator
Article
Colombia
Cystic fibrosis
Disease association
Gene frequency
Gene mutation
Human
Major clinical study
Mexico
Priority journal
Venezuela
Colombia
Cystic fibrosis
Cystic fibrosis transmembrane conductance regulator
Gene frequency
Humans
Mexico
Mutation
Prevalence
Spain
Venezuela
Allele/mutation frequencies
Cystic fibrosis
Ethnic groups
Latin america
description We analyzed 192 cystic fibrosis (CF) alleles in three Latin American countries: Mexico, Colombia, and Venezuela. Mutation screening was performed by polymerase chain reaction (PCR) and a reverse dot blot detection kit that enables determination of 16 of the most common CF mutations worldwide. Mutations were detected in 47.9% of the screened CF alleles. The most prevalent CF allele was ?F508 (39.6%). The remaining 16 non-?F508 detectable mutations represented 8.3% of the CF alleles. Among them, the G542X, N1303K, and 3849+10kb C > T were the most common. Although the frequency of ?F508 described here is lower than that reported for Caucasian populations, including in Spain, it is remarkable that mutation prevalences found in this study resemble those observed in Spain. Two of these mutations, G542X and 3849+10kb C>T, that were relevant in this analysis, have a particularly high incidence in Spanish communities. The low frequency of ?F508 described here may be explained by the Amerindian, Caucasian, and Black admixture that occurred in Latin America after the discovery of the New World, and also by the probable occurrence of mutations contributed by the original natives, which were undetectable in this analysis. (C) 2000 Wiley- Liss, Inc.
publishDate 2000
dc.date.created.spa.fl_str_mv 2000
dc.date.accessioned.none.fl_str_mv 2020-06-11T13:22:29Z
dc.date.available.none.fl_str_mv 2020-06-11T13:22:29Z
dc.type.eng.fl_str_mv article
dc.type.coarversion.fl_str_mv http://purl.org/coar/version/c_970fb48d4fbd8a85
dc.type.coar.fl_str_mv http://purl.org/coar/resource_type/c_6501
dc.type.spa.spa.fl_str_mv Artículo
dc.identifier.doi.none.fl_str_mv https://doi.org/10.1002/(SICI)1096-8628(20000410)91:4<277::AID-AJMG7>3.0.CO;2-A
dc.identifier.uri.none.fl_str_mv https://repository.urosario.edu.co/handle/10336/25139
url https://doi.org/10.1002/(SICI)1096-8628(20000410)91:4<277::AID-AJMG7>3.0.CO;2-A
https://repository.urosario.edu.co/handle/10336/25139
dc.language.iso.none.fl_str_mv eng
language eng
dc.relation.citationEndPage.none.fl_str_mv 279
dc.relation.citationIssue.none.fl_str_mv No. 4
dc.relation.citationStartPage.none.fl_str_mv 277
dc.relation.citationTitle.none.fl_str_mv American Journal of Medical Genetics
dc.relation.citationVolume.none.fl_str_mv Vol. 91
dc.relation.ispartof.spa.fl_str_mv American Journal of Medical Genetics, ISSN:, Vol.91, No.4 (2000); pp. 277-279
dc.relation.uri.spa.fl_str_mv https://onlinelibrary.wiley.com/doi/abs/10.1002/%28SICI%291096-8628%2820000410%2991%3A4%3C277%3A%3AAID-AJMG7%3E3.0.CO%3B2-A
dc.rights.coar.fl_str_mv http://purl.org/coar/access_right/c_14cb
dc.rights.acceso.spa.fl_str_mv Bloqueado (Texto referencial)
rights_invalid_str_mv Bloqueado (Texto referencial)
http://purl.org/coar/access_right/c_14cb
dc.format.mimetype.none.fl_str_mv application/pdf
dc.publisher.spa.fl_str_mv American Journal of Medical Genetics
institution Universidad del Rosario
dc.source.instname.spa.fl_str_mv instname:Universidad del Rosario
dc.source.reponame.spa.fl_str_mv reponame:Repositorio Institucional EdocUR
repository.name.fl_str_mv Repositorio institucional EdocUR
repository.mail.fl_str_mv edocur@urosario.edu.co
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