2010•International Journal of Pediatric OtorhinolaryngologyRequires access

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

Halima Nahili, Majida Charif, Redouane Boulouiz, Safaa Bounaceur, Houda Benrahma, Omar Abidi, Abdelaziz Chafik, Hassan Rouba, Mostafa Kandil, Abdelhamid Barakat

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Key concepts: Haplogroup, Mitochondrial DNA, Medicine, Sensorineural hearing loss, Hearing loss, Genetics, Mutation, Polymorphism (computer science)

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Prevalence of the mitochondrial A 1555G mutation in Moroccan patients with non-syndromic hearing loss — Research Paper | ScholarLens