Lv1
10 积分 2025-10-17 加入
Clinical application of whole exome sequencing (WES) in the genetic diagnosis of 768 Chinese patients with bilateral hearing loss
3个月前
已完结
Mechano-electrical transduction components TMC1-CIB2 undergo a Ca2+-induced conformational change linked to hearing loss
4个月前
已完结
Targeted Next-Generation Sequencing Analysis Reveals a Novel Genetic Variant in MYO6 Gene in an Indian Family with Postlingual Nonsyndromic Hearing Loss
5个月前
已完结
Genetic etiology of non-syndromic hearing loss in Europe
5个月前
已完结
Differential disruption of autoinhibition and defect in assembly of cytoskeleton during cell division decide the fate of humanDIAPH1-related cytoskeletopathy
5个月前
已完结
A novel frameshift mutation in the DIAPH1 gene causes a Chinese family autosomal dominant nonsyndromic hearing loss
5个月前
已完结
Genetic analysis of patients with low-frequency non-syndromic hearing loss
5个月前
已完结
Identification of a novel DFNA5 mutation, IVS7-2 a > G, in a Chinese family with non-syndromic sensorineural hearing loss
5个月前
已完结
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