Prevalence of the mitochondrial A 1555G mutation in Moroccan patients with non-syndromic hearing loss.

Halima Nahili,M. Charif,Redouane Boulouiz,Safaa Bounaceur,H. Benrahma,O. Abidi,A. Chafik,H. Rouba,M. Kandil,A. Barakat

Published 2010 in International Journal of Pediatric Otorhinolaryngology

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