The Relationship between the p.V37I Mutation in GJB2 and Hearing Phenotypes in Chinese Individuals

The most common cause of nonsyndromic autosomal recessive hearing loss is mutations in GJB2. The mutation spectrum and prevalence of mutations vary significantly among ethnic groups, and the relationship between p.V37I mutation in GJB2 and the hearing phenotype is controversial. Among the 3,864 pati...

Descripción completa

Detalles Bibliográficos
Autores principales: Huang, Shasha, Huang, Bangqing, Wang, Guojian, Yuan, Yongyi, Dai, Pu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4463851/
https://www.ncbi.nlm.nih.gov/pubmed/26061099
http://dx.doi.org/10.1371/journal.pone.0129662

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4463851/
https://www.ncbi.nlm.nih.gov/pubmed/26061099
http://dx.doi.org/10.1371/journal.pone.0129662

Ejemplares similares