Lv731
4510 积分 2023-10-11 加入
Homozygous variants in WDR83OS lead to a neurodevelopmental disorder with hypercholanemia
4天前
已完结
Homozygous variants in WDR83OS lead to a neurodevelopmental disorder with hypercholanemia
5天前
已完结
A narrative review on periprocedural stroke and transcatheter aortic valve replacement: Achilles' heel
8个月前
已完结
Elastin architecture
8个月前
已完结
A homozygous variant in INTS11 links mitosis and neurogenesis defects to a severe neurodevelopmental disorder
9个月前
已完结
KATP channel mutation disrupts hippocampal network activity and nocturnal gamma shifts
10个月前
已完结
De novo variants in ATXN7L3 lead to developmental delay, hypotonia and distinctive facial features
10个月前
已完结
Clinical and functional consequences of GRIA variants in patients with neurological diseases
11个月前
已完结
De novo CLPTM1 variants with reduced GABAAR current response in patients with epilepsy
11个月前
已完结
PACS gene family-related neurological diseases: limited genotypes and diverse phenotypes
11个月前
已完结
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