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...

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Detalles Bibliográficos
Autores principales: Kaheel, Hazem, Breß, Andreas, Hassan, Mohamed A., Shah, Aftab Ali, Amin, Mutaz, Bakhit, Yousuf H. Y., Kniper, Marlies
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5736926/
https://www.ncbi.nlm.nih.gov/pubmed/29362677
http://dx.doi.org/10.1155/2017/5836525

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5736926/
https://www.ncbi.nlm.nih.gov/pubmed/29362677
http://dx.doi.org/10.1155/2017/5836525

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