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A novel frameshift mutation (c.405delC) in the GJB2 gene associated with autosomal recessive hearing loss in two Tunisian families

✍ Scribed by Riahi, Zied; Chahed, Houda; Jaafoura, Habib; Zainine, Rim; Messaoud, Olfa; Naili, Mohamed; Nagara, Majdi; Hammami, Hassan; Laroussi, Nadia; Bouyacoub, Yosra; Kefi, Rym; Bonnet, Crystel; Besbes, Ghazi; Abdelhak, Sonia

Book ID: 120571375
Publisher: Elsevier Science
Year: 2013
Tongue: English
Weight: 619 KB
Volume: 77
Category: Article
ISSN: 0165-5876
DOI: 10.1016/j.ijporl.2013.06.015

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