A novel de novo mutation of ACTG1 in two sporadic non-syndromic hearing loss cases.
Wang H, Guan J, Lan L, Yu L, Xie L, Liu X, Yang J, Zhao C, Wang D, Wang Q.
Wang H, et al. Among authors: wang d, wang q.
Sci China Life Sci. 2018 Jun;61(6):729-732. doi: 10.1007/s11427-017-9165-2. Epub 2018 Jan 2.
Sci China Life Sci. 2018.
PMID: 29357087
No abstract available.