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Autosomal Recessive Nonsyndromic Hearing Loss: A Case Report with a Mutation in TRIOBP Gene

Hearing loss (HL) is the most common sensory defect. Various genetic as well as environmental factors have been shown to contribute in it. More than 100 loci have been recognized to cause autosomal recessive nonsyndromic hearing loss (ARNSHL). Here, we report a 6-year old female patient with bilater...

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Библиографические подробности
Опубликовано в: :Int J Mol Cell Med
Главные авторы: Fardaei, Majid, Sarrafzadeh, Shaghayegh, Ghafouri-Fard, Soudeh, Miryounesi, Mohammad
Формат: Artigo
Язык:Inglês
Опубликовано: Babol University of Medical Sciences 2015
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Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC4769603/
https://ncbi.nlm.nih.gov/pubmed/27014650
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