Frequency of c.35delG Mutation in GJB2 Gene (Connexin 26) in Syrian Patients with Nonsyndromic Hearing Impairment

BACKGROUND: Hearing impairments (HI) are the most common birth defect worldwide. Very large numbers of genes have been identified but the most profound is GJB2. The clinical interest regarding this gene is very pronounced due to its high carrier frequency (0.5–5.4%) across different ethnic groups. T...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:Genet Res Int
Main Authors: Kaheel, Hazem, Breß, Andreas, Hassan, Mohamed A., Shah, Aftab Ali, Amin, Mutaz, Bakhit, Yousuf H. Y., Kniper, Marlies
Formato: Artigo
Idioma:Inglês
Publicado em: Hindawi 2017
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5736926/
https://ncbi.nlm.nih.gov/pubmed/29362677
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2017/5836525
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados