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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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Genet Res Int
Prif Awduron: Kaheel, Hazem, Breß, Andreas, Hassan, Mohamed A., Shah, Aftab Ali, Amin, Mutaz, Bakhit, Yousuf H. Y., Kniper, Marlies
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Hindawi 2017
Pynciau:
Research Article
Mynediad Ar-lein: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
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