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0 积分 2025-10-17 加入
Genetic etiology of non-syndromic hearing loss in Europe
2小时前
已完结
Differential disruption of autoinhibition and defect in assembly of cytoskeleton during cell division decide the fate of humanDIAPH1-related cytoskeletopathy
8小时前
已完结
A novel frameshift mutation in the DIAPH1 gene causes a Chinese family autosomal dominant nonsyndromic hearing loss
8小时前
已完结
Genetic analysis of patients with low-frequency non-syndromic hearing loss
9小时前
已完结
Identification of a novel DFNA5 mutation, IVS7-2 a > G, in a Chinese family with non-syndromic sensorineural hearing loss
12小时前
已完结
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