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Absence of GJB3 and GJB6 mutations in Moroccan familial and sporadic patients with autosomal recessive non-syndromic deafness

✍ Scribed by Halima Nahili; Mohamed Ridal; Redouane Boulouiz; Omar Abidi; Laila Imken; Hassan Rouba; Mohammed Noureddine Alami; Abdelaziz Chafik; Mohammed Hassar; Abdelhamid Barakat

Book ID: 116565005
Publisher: Elsevier Science
Year: 2008
Tongue: English
Weight: 116 KB
Volume: 72
Category: Article
ISSN: 0165-5876
DOI: 10.1016/j.ijporl.2008.07.015

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