Lv31
300 积分 2022-03-07 加入
Clinical Aspects of Usher Syndrome and theUSH2AGene in a Cohort of 433 Patients
5小时前
待确认
Novel Mutation in the Homeobox Domain of Transcription Factor POU3F4 Associated With Profound Sensorineural Hearing Loss
5天前
已完结
A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh-1 gene
17天前
已完结
SCUBE3 Exerts a Tumor-Promoting Effect in Tongue Squamous Cell Carcinoma by Promoting CEBPA Binding to the CCL2 Promoter
4个月前
已完结
PHENOTYPIC CHARACTERISTICS OF ROD–CONE DYSTROPHY ASSOCIATED WITH MYO7A MUTATIONS IN A LARGE FRENCH COHORT
7个月前
已完结
Select autosomal dominant DFNA11 deafness mutations activate Myo7A targeting in epithelial cells
7个月前
已关闭
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