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DFNB59 gene

Known as: PJVK, DFNB59, PEJVAKIN 
National Institutes of Health

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DEAFNESS, AUTOSOMAL RECESSIVE 59DFNB60 gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Gene Therapy for Hearing and Balance defects : How close are we ?
Since the initial report on hearing restoration by cochlear gene transfer in a mouse mutant defective for vesicular gluta-mate… 
2015
2015
بررسی پیوستگی ژنتیکی لوکوس DFNB59 و ناشنوایی غیرسندرمی مغلوب اتوزومی در خانوادههایی از استانهای غربی کشور
2013
2013
Distribution of pejvakin in human spiral ganglion: An immunohistochemical study
Abstract Up to 10% of permanent hearing impairments in children originate from lesions in the neuronal auditory pathway. This… 
2012
2012
مطالعه ناشنوايي وابسته به موتاسيونهاي ژن DFNB59 (پژواکين) در جمعيتهاي ناشنواي استان فارس
Background and Objectives: Hearing loss is the most frequent sensory disorder affecting 1 in 500 neonates with more than 50% of… 
Review
2011
Review
2011
Genetic Update on Auditory Neuropathy
Auditory neuropathy (AN) is defined as a sensorineural hearing impairment (HI) characterized by preserved cochlear outer hair… 
2011
2011
مطالعه ناشنوایی وابسته به موتاسیونهای ژن DFNB59 (پژواکین) در جمعیتهای ناشنوای استان فارس
1 . كيتنژ سانشراك ، يلولس تاقيقحت زكرم و يلوكلم ، يكشزپ مولع هاگشناد يتشادهب تامدخ و ينامرد دركرهش 2… 
2010
2010
بررسی جهشهای ژن DFNB59 با استفاده از روش PCR-SSCP/HA در ناشنوایی ژنتیکی غیرسندرمی در استان بوشهر
2009
2009
Trends in Genetic Research on Auditory Neuropathy
Various etiologies of auditory neuropathy (AN) have been reported, including genetic causes. Genes such as OTOF and pejvakin… 
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