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GJB2 (connexin 26) gene mutations in Moroccan patients with autosomal recessive non-syndromic hearing loss and carrier frequency of the common GJB2–35delG mutation

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

Book ID: 116564608
Publisher: Elsevier Science
Year: 2007
Tongue: English
Weight: 365 KB
Volume: 71
Category: Article
ISSN: 0165-5876
DOI: 10.1016/j.ijporl.2007.04.019

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