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...
- 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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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 |
_version_ |
1814167711690784768 |