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Mutation analysis of GJB2 and GJB6 genes and screening of nine common dfnb loci in iranian pedigrees with autosomal recessive nonsyndromic hearing loss

Azadegan-Dehkordi Fatemeh, Koohiyan Mahbobeh, Shirzad Maryam, Bahrami Tayyeb, Yazdanpanahi Nasrin, Tabatabaiefar Mohammad Amin, Pourpaknia Reza, Farrokhi Effat, Hashemzadeh-Chaleshtori Morteza

Year : 2019| Volume: 25| Issue : 2 | Page no: 97-102

   This article has been cited by
1 Molecular diagnosis of SLC26A4-related hereditary hearing loss in a group of patients from two provinces of Iran
Mahbobeh Koohiyan,Morteza Hashemzadeh-Chaleshtori,Mohammad Amin Tabatabaiefar
Intractable & Rare Diseases Research. 2020;
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