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30 积分 2022-03-31 加入
Gain-of-function p.F28S variant inRAC3disrupts neuronal differentiation, migration and axonogenesis during cortical development, leading to neurodevelopmental disorder
10小时前
求助中
The role of copy number variants in the genetic architecture of common familial epilepsies
2个月前
已完结
Common genes and recurrent causative variants in 957 Asian patients with pediatric epilepsy
2个月前
已完结
KCNT2‐Related Disorders: Phenotypes, Functional, and Pharmacological Properties
2个月前
已完结
Podocyte-specific Nup160 knockout mice develop nephrotic syndrome and glomerulosclerosis
2个月前
已关闭
Genetic Testing In Pediatric Epilepsy: Tools, Tips And Navigating The Traps
3个月前
已完结
mTOR and neuroinflammation in epilepsy: implications for disease progression and treatment
8个月前
已完结
Channelopathies in epilepsy: an overview of clinical presentations, pathogenic mechanisms, and therapeutic insights
8个月前
已完结
Improving epilepsy diagnosis across the lifespan: approaches and innovations
8个月前
已完结
The current landscape of epilepsy genetics: where are we, and where are we going?
10个月前
已完结
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