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DEAFNESS, AUTOSOMAL RECESSIVE 29

Known as: DFNB29 
National Institutes of Health

Related topics

Related topics

2 relations
Autosomal recessive inheritanceCLDN14, VAL85ASP

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
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…
Background: We aimed to determine the contribution of four DFNB loci and mutation analysis of gap junction beta-2 (GJB2) and GJB4… 
2010
2010
Haplotype Analysis of Seven Non-Syndromeic Autosomal Recessive Hearing Loss Loci in Iranian Families
Objective: Hearing impairment is the most frequent sensorineural defect in 2 forms, syndromic and non–syndromic. The aim of this… 
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