Genetic and clinical analysis of nonsyndromic hearing impairment in pediatric and adult cases

Previous studies have linked GJB2 gene and mitochondrial DNA (mtDNA) mutations to nonsyndromic hearing impairment (NSHI), but no study in China has yet investigated these mutations across all age groups. To fill the gap, this study ascertained 263 patients with NSHI between ages 2 months and 60 year...

Descripción completa

Detalles Bibliográficos
Autores principales: Xing, J, Liu, X, Tian, Y, Tan, J, Zhao, H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: De Gruyter 2016
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5026278/
https://www.ncbi.nlm.nih.gov/pubmed/27785406
http://dx.doi.org/10.1515/bjmg-2016-0005

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5026278/
https://www.ncbi.nlm.nih.gov/pubmed/27785406
http://dx.doi.org/10.1515/bjmg-2016-0005

Ejemplares similares