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High carrier frequency of the GJB2 mutation (35delG) in the north of Iran

✍ Scribed by Morteza Hashemzadeh Chaleshtori; Effat Farrokhi; Mehrdad Shahrani; Soleiman Kheiri; Masoumeh Dolati; Laleh Hoghooghi Rad; Hamid Pour-Jafari; Keihan Ghatreh Samani; Katayoon Safa Chaleshtori; Andrew H. Crosby

Book ID: 116564540
Publisher: Elsevier Science
Year: 2007
Tongue: English
Weight: 298 KB
Volume: 71
Category: Article
ISSN: 0165-5876
DOI: 10.1016/j.ijporl.2007.02.005

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## Abstract Mutations in __GJB2__ are a major cause of autosomal recessive non‐syndromic hearing loss (ARNSHL) in many populations. A single mutation of this gene (35delG) accounts for approximately 70% of __GJB2__ mutations that are associated with ARNSHL in Caucasians in many European countries a

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