Screening for the mitochondrial A1555G mutation among Egyptian patients with non-syndromic, sensorineural hearing loss

Background & Aim: Hearing loss is the most frequent form of neurosensory deficit in humans. Although the majority of hereditary hearing loss is due to nuclear gene mutations, it has become clear the significant contribution of mitochondrial genes. The first mitochondrial mutation shown to cause...

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Bibliographic Details
Published in:Int J Mol Epidemiol Genet
Main Authors: Fassad, Mahmoud R, Desouky, Lubna M, Asal, Samir, Abdalla, Ebtesam M
Format: Artigo
Language:Inglês
Published: e-Century Publishing Corporation 2014
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Original Article
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC4348701/
https://ncbi.nlm.nih.gov/pubmed/25755848
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