Mutations of human TMHS cause recessively inherited non-syndromic hearing loss.
人类TMHS基因突变会导致隐性遗传的非综合征性听力损失
期刊:Journal of Medical Genetics
影响因子:3.7
doi:10.1136/jmg.2005.039834
Shabbir M I, Ahmed Z M, Khan S Y, Riazuddin Saima, Waryah A M, Khan S N, Camps R D, Ghosh M, Kabra M, Belyantseva I A, Friedman T B, Riazuddin Sheikh
