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Deafness; Ear; Transmembrane channel-like 1; Hearing loss; Missense mutation
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doi:10.1186/s12967-016-0780-5
BioMed Central
Journal of Translational Medicine, doi:10.1186/s12967-016-0780-5
Deafness; Ear; Transmembrane channel-like 1; Hearing loss; Missense mutation
Exome sequencing identifies a mutation in TMC1 as a novel cause of autosomal recessive nonsyndromic hearing loss
Jiongjiong Hu
Fei Liu
Wenjun Xia
Lili Hao
Jun Lan
Zhenghua Zhu
Jing Ye
Duan Ma
Zhaoxin Ma
10.1186/s12967-016-0780-5
2010-04-23
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