Lv3
260 积分 2022-11-20 加入
Epilepsy-associated genes: an update
5天前
已完结
LRPPRC mutations cause a phenotypically distinct form of Leigh syndrome with cytochrome c oxidase deficiency
2个月前
已完结
The clinical and genetic landscape of developmental and epileptic encephalopathies in Egyptian children
3个月前
已完结
Genetic analysis of developmental and epileptic encephalopathy caused by novel biallelic SZT2 gene mutations in three Chinese Han infants: a case series and literature review
3个月前
已完结
Developmental and epileptic encephalopathies
3个月前
已完结
Biallelic variants of KCNQ2 in early infantile developmental and epileptic encephalopathy
3个月前
已完结
Association of LONP1 gene with epilepsy and the sub-regional effect
4个月前
已完结
CCDC22 variants caused X-linked focal epilepsy and focal cortical dysplasia
4个月前
已完结
ARHGAP4 variants are associated with X-linked early-onset temporal lobe epilepsy
6个月前
已完结
Giant ankyrin-B suppresses stochastic collateral axon branching through direct interaction with microtubules
7个月前
已完结
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