Next generation sequencing and genetics of hereditary hearing loss in the iranian population: New insights from a systematic review
Author:
Publisher
Elsevier BV
Subject
Otorhinolaryngology,General Medicine,Pediatrics, Perinatology and Child Health
Reference35 articles.
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4. Screening for MYO15A gene mutations in autosomal recessive nonsyndromic, GJB2 negative Iranian deaf population;Fattahi;Am. J. Med. Genet.,2012
5. AUNA2: a novel type of non-syndromic slowly progressive auditory synaptopathy/auditory neuropathy with autosomal-dominant inheritance;Lang-Roth;Audiol. Neurotol.,2017
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