Exome sequencing identifies a mutation in TMC1 as a novel cause of autosomal recessive nonsyndromic hearing loss
Crossref DOI link: https://doi.org/10.1186/s12967-016-0780-5
Published Online: 2016-01-28
Published Print: 2016-12
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Hu, Jiongjiong
Liu, Fei
Xia, Wenjun
Hao, Lili
Lan, Jun
Zhu, Zhenghua
Ye, Jing
Ma, Duan
Ma, Zhaoxin