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DEAFNESS, AUTOSOMAL RECESSIVE 29
Known as:
DFNB29
National Institutes of Health
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Related topics
Related topics
2 relations
Autosomal recessive inheritance
CLDN14, 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…
Masoud Akbarzadeh Laleh
,
Marzieh Naseri
,
+5 authors
A. Nejatizadeh
Journal of Research in Medical Sciences
2017
Corpus ID: 8061067
Background: We aimed to determine the contribution of four DFNB loci and mutation analysis of gap junction beta-2 (GJB2) and GJB4…
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2010
2010
Haplotype Analysis of Seven Non-Syndromeic Autosomal Recessive Hearing Loss Loci in Iranian Families
R. Badr
,
Bahareh Shoja-Saffar
,
Niloofar Bazzaz-Zadegan
,
K. Jalalvand
,
K. Kahrizi
,
H. Najmabadi
2010
Corpus ID: 74347238
Objective: Hearing impairment is the most frequent sensorineural defect in 2 forms, syndromic and non–syndromic. The aim of this…
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