Lv1
40 积分 2026-02-01 加入
Analysis of clinical features and genetic variants in Chinese children with pyridoxine-dependent epilepsy: a case series study
1个月前
已完结
Deleterious, protein-altering variants in GSPT2 are putatively associated with an X-linked neurodevelopmental disorder with intellectual disability, language impairment, autism and epilepsy
1个月前
已关闭
Deleterious, protein-altering variants in GSPT2 are putatively associated with an X-linked neurodevelopmental disorder with intellectual disability, language impairment, autism and epilepsy
2个月前
已关闭
皖公网安备34019202002308
