Lv41
450 积分 2025-10-28 加入
[Analysis of clinical phenotype and genetic variants in a child with mitochondrial F-S disease due to variants of FDXR gene]
5小时前
待确认
[Genetic analysis of a child with early onset neurodevelopmental disorder with involuntary movement and a literature review]
5小时前
已完结
[Genetic analysis of a child with Leukoencephalopathy with ataxia caused by a homozygous variant of CLCN2 gene and a literature review]
6小时前
已完结
A novel splicing variant in MICAL-1 gene is associated with epilepsy
6小时前
已完结
A Novel m.1636A > G Variant in Mitochondrial TV Gene Might Cause New Phenotype of Mitochondrial Disease in a 2-Year Old Chinese Boy
6小时前
已完结
HCN1 pathogenic variants associated with childhood epilepsy in a cohort of Chinese patients
6小时前
已完结
Homer/vesl proteins and their roles in CNS neurons
1个月前
已完结
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