Análisis Molecular de las Mutaciones 2299delG y C759F en Individuos Colombianos con Retinitis Pigmentosa e Hipoacusia Neurosensorial

Objective: To determine the presence of 2299delG and C759F mutations in 37 non-related subjects from Colom­bia suffering from RP and sensorineural deafness. Materials and methods:Exon 13 of USH2A gene was directly sequenced in all subjects selected for the study. Results: In this work, the 2299delG...

Full description

Autores:

Greizy López
Nancy Yaneth Gelvez
Luisa Fernanda Urrego
Silvia Florez
David Medina
Vicente Rodríguez
Marta Lucía Tamayo

Tipo de recurso:

Article of investigation

Fecha de publicación:

2015

Institución:

Colegio Mayor de Cundinamarca

Repositorio:

Repositorio Colegio Mayor de Cundinamarca

Idioma:

spa

OAI Identifier:

oai:repositorio.unicolmayor.edu.co:unicolmayor/4370

Acceso en línea:

https://doi.org/10.22490/24629448.1038
https://repositorio.unicolmayor.edu.co/handle/unicolmayor/4370

Palabra clave:

Rights

openAccess

License

https://creativecommons.org/licenses/by/4.0/