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

✍ Scribed by Halima Nahili; Majida Charif; Redouane Boulouiz; Safaa bounaceur; Houda Benrahma; Omar Abidi; Abdelaziz Chafik; Hassan Rouba; Mostafa Kandil; Abdelhamid Barakat

Book ID: 116565692
Publisher: Elsevier Science
Year: 2010
Tongue: English
Weight: 237 KB
Volume: 74
Category: Article
ISSN: 0165-5876
DOI: 10.1016/j.ijporl.2010.06.008

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