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70 积分 2025-07-23 加入
Mutations in the WFS1 gene are a frequent cause of autosomal dominant nonsyndromic low-frequency hearing loss in Japanese
3个月前
已完结
[Mutation analysis for a Chinese family featuring X-linked alpha thalassemia/mental retardation syndrome]
7个月前
已完结
Mutation spectrum and genotype-phenotype correlations in 157 Korean CADASIL patients: a multicenter study
9个月前
已完结
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