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246 积分 2024-11-21 加入
Phenotype-genotype analysis of the autosomal recessive hereditary hearing loss caused by OTOA variations
4天前
已完结
Arrhythmic Phenotypes Are a Defining Feature of Dilated Cardiomyopathy-Associated SCN5A Variants: A Systematic Review
30天前
已完结
Low Penetrance Sarcomere Variants Contribute to Additive Risk in Hypertrophic Cardiomyopathy
1年前
已完结
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