日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

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

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

Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafness

东亚和南亚人群中SLC26A4 (PDS) 基因突变的起源和频率:对耳聋流行病学的全球意义

Park, H-J; Shaukat, S; Liu, X-Z; Hahn, S H; Naz, S; Ghosh, M; Kim, H-N; Moon, S-K; Abe, S; Tukamoto, K; Riazuddin, S; Kabra, M; Erdenetungalag, R; Radnaabazar, J; Khan, S; Pandya, A; Usami, S-I; Nance, W E; Wilcox, E R; Riazuddin, S; Griffith, A J