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Deafness, Autosomal Recessive 21

Known as: DFNB21 
National Institutes of Health

Related topics

Related topics

2 relations
Autosomal recessive inheritance

Broader (1)

Sensorineural Hearing Loss (disorder)

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… 
2017
2017
مطالعه و تجزیه و تحلیل پیوستگی ژنتیکی لوکوس DFNB21 در بیماری ناشنوایی مغلوب آتوزومی در خانوادههای بزرگ استان خوزستان
2016
2016
Genetic Linkage Analysis of DFNB3, DFNB9 and DFNB21 Loci in GJB2 Negative Families with Autosomal Recessive Non-syndromic Hearing Loss
Background: Autosomal recessive non-syndromic hearing loss (ARNSHL) is the most common hereditary form of deafness, and exhibits… 
2012
2012
A commentary on ‘TECTA mutations in Japanese with mid-frequency hearing loss affected by Zona Pellucida domain protein secretion’
A commentary on ‘ TECTA mutations in Japanese with mid-frequency hearing loss affected by Zona Pellucida domain protein secretion… 
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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