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Three MYO15A Mutations Identified in One Chinese Family with Autosomal Recessive Nonsyndromic Hearing Loss

Hearing impairment is one of the most common sensory disease, of which more than 50% is attributed to a genetic etiology. The goal of this research is to explore the genetic cause of a Chinese deafness pedigree who was excluded of GJB2, SLC26A4, or MtDNA12SrRNA variants. Three variants, c.3971C>A...

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Detaylı Bibliyografya
Yayımlandı:Neural Plast
Asıl Yazarlar: Zhang, Fengguo, Xu, Lei, Xiao, Yun, Li, Jianfeng, Bai, Xiaohui, Wang, Haibo
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Hindawi 2018
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5907479/
https://ncbi.nlm.nih.gov/pubmed/29849560
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2018/5898025
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