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Targeted Gene Capture and Massively Parallel Sequencing Identify TMC1 as the Causative Gene in a Six-generation Chinese Family with Autosomal Dominant Hearing Loss

Hereditary nonsyndromic hearing loss is extremely heterogeneous. Mutations in the transmembrane channel-like gene1 (TMC1) are known to cause autosomal dominant and recessive forms of nonsyndromic hearing loss linked to the loci of DFNA36 and DFNB7/11, respectively. We characterized a six-generation...

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Detaylı Bibliyografya
Yayımlandı:Am J Med Genet A
Asıl Yazarlar: Gao, Xue, Huang, Sha-Sha, Yuan, Yong-Yi, Wang, Guo-Jian, Xu, Jin-Cao, Ji, Yu-Bin, Han, Ming-Yu, Yu, Fei, Kang, Dong-Yang, Lin, Xi, Dai, Pu
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2015
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4567392/
https://ncbi.nlm.nih.gov/pubmed/26079994
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.37206
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