Lv21
150 积分 2025-09-18 加入
Post-mortem genetic analysis of sudden unexplained death in a young cohort: a whole-exome sequencing study
2小时前
待确认
HOGA1 variants in Chinese patients with primary hyperoxaluria type 3: genetic features and genotype-phenotype relationships
1个月前
已完结
A novel phenotype of AChR-deficiency syndrome with predominant facial and distal weakness resulting from the inclusion of an evolutionary alternatively-spliced exon in CHRNA1
10个月前
已完结
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