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DEAFNESS, AUTOSOMAL RECESSIVE 59

Known as: DFNB59 
National Institutes of Health

Related topics

Related topics

4 relations
Autosomal recessive inheritanceDFNB59 geneDFNB59, ARG183TRP

Broader (1)

Sensorineural Hearing Loss (disorder)

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Mutation analysis of GJB2 and GJB6 genes and screening of nine common dfnb loci in iranian pedigrees with autosomal recessive nonsyndromic hearing loss
Background: Hearing loss (HL) is one of the most common sensory disorders (1/1000). Various studies have shown that a large… 
2015
2015
بررسی پیوستگی ژنتیکی لوکوس DFNB59 و ناشنوایی غیرسندرمی مغلوب اتوزومی در خانوادههایی از استانهای غربی کشور
2014
2014
بررسی آنالیز پیوستگی برای جایگاه شایع DFNB59 در بین 36 خانواده ی ایرانی مبتلا به ناشنوایی غیرسندرمی با توارث اتوزوم مغلوب
2011
2011
Study of Deafness Associated with DFNB59 Gene (pejvakin) Mutation in Fars Province
2010
2010
DFNB59 GENE MUTATIONS AND ITS ASSOCIATION WITH DEAFNESS IN SCHOOLCHILDREN IN KOHGILOOYEH & BOYERAHMAD PROVINCE
Introduction & Objective: Hearing loss is a common disease affecting millions of people worldwide. Hearing loss can be caused… 
2010
2010
DFNB59 GENE MUTATION SCREENING USING PCR-SSCP/HA TECHNIQUE IN NON-SYNDROMIC GENETIC HEARING LOSS IN BUSHEHR PROVINCE
Background: Hearing impairment (HI) is the most prevalent Neurosensory disorder which is heterogenous and can also occur due to… 
2010
2010
THE CONTRIBUTION OF AUTOSOMAUL RECESSIVE NON-SYNDROMIC DEAFNESS TO DFNB59 MUTATIONS (PEJVAKIN)
2010
2010
بررسی جهشهای ژن DFNB59 با استفاده از روش PCR-SSCP/HA در ناشنوایی ژنتیکی غیرسندرمی در استان بوشهر
2009
2009
Study of DFNB59 gene mutations in exon 2 and 4 in association with deafness using PCR-RFLP in Chaharmahal va Bakhtiari, Iran
2009
2009
بررسی جهش های اگزون 2 و 4 ژن پژواکین (DFNB59) در ارتباط با ناشنوایی با استفاده از PCR-RFLP در استان چهارمحال و بختیاری
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