Identification of Novel TMC1 Compound Heterozygous Mutations Related to Autosomal Recessive Hearing Loss by Targeted Capture Sequencing

Identification of Novel TMC1 Compound Heterozygous Mutations Related to Autosomal Recessive Hearing Loss by Targeted Capture Sequencing

<p>Mutations in the transmembrane channel-like gene1 (TMC1) are known to cause autosomal dominant and recessive forms of nonsyndromic hearing loss DFNA36 and vDFNB7/11, respectively. Here, we characterized a 5-year old girl with severe sensorineural hearing loss. By combining targeted capture...

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Bibliographic Details
Main Authors:	Xue Gao (Author), Sha-Sha Huang (Author), Yu Su (Author), Jin-Cao Xu (Author), Pu Dai (Author)
Format:	Book
Published:	Scientific Journal of Genetics and Gene Therapy - Peertechz Publications, 2016-07-08.
Subjects:	Research Article
Online Access:	Connect to this object online.
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