Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss
Wolfram综合征1基因(WFS1)突变是低频感音神经性听力损失的常见原因。
期刊:Human Molecular Genetics
影响因子:3.2
doi:10.1093/hmg/10.22.2501
Bespalova, I N; Van Camp, G; Bom, S J; Brown, D J; Cryns, K; DeWan, A T; Erson, A E; Flothmann, K; Kunst, H P; Kurnool, P; Sivakumaran, T A; Cremers, C W; Leal, S M; Burmeister, M; Lesperance, M M