A rare novel mutation in TECTA causes autosomal dominant nonsyndromic hearing loss in a Mongolian family

BACKGROUND: The genetic basis of autosomal dominant nonsyndromic hearing loss is complex. Genetic factors are responsible for approximately 50% of cases with congenital hearing loss. However, no previous studies have documented the clinical phenotype and genetic basis of autosomal dominant nonsyndro...

Descripción completa

Detalles Bibliográficos
Autores principales: Bai, Haihua, Yang, Xukui, Temuribagen, Guilan, Suyalatu, Narisu, Narisu, Wu, Huiguang, Chen, Yujie, Liu, Yangjian, Wu, Qizhu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3994966/
https://www.ncbi.nlm.nih.gov/pubmed/25008054
http://dx.doi.org/10.1186/1471-2350-15-34

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3994966/
https://www.ncbi.nlm.nih.gov/pubmed/25008054
http://dx.doi.org/10.1186/1471-2350-15-34

Ejemplares similares