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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Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Genet Res Int
Päätekijät: Kaheel, Hazem, Breß, Andreas, Hassan, Mohamed A., Shah, Aftab Ali, Amin, Mutaz, Bakhit, Yousuf H. Y., Kniper, Marlies
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Hindawi 2017
Aiheet:
Research Article
Linkit: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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