ArticleJournal of research in medical sciences : the official journal of Isfahan University of Medical Sciences2017

Diverse pattern of gap junction beta-2 and gap junction beta-4 genes mutations and lack of contribution of DFNB21, DFNB24, DFNB29, and DFNB42 loci in autosomal recessive nonsyndromic hearing loss patients in Hormozgan, Iran.

Masoud Akbarzadeh Laleh et al.PubMed ↗Full text ↗Publisher ↗

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