Lv11
40 积分 2024-12-18 加入
Immune evasion and ACE2 binding affinity contribute to SARS-CoV-2 evolution
6小时前
待确认
Age at onset of genetic disease and genetic dependent stage: evidence from cases with SCN1A variants
1个月前
已完结
[De novo variant of CSNK2B causes Poirier-Bienvenu neurodevelopmental syndrome: two case report]
2个月前
已关闭
[Progressive Myoclonus Epilepsy: Diversity of Disorders and Key Points in Clinical Practice]
2个月前
已关闭
CSNK2B splice site mutations in patients cause intellectual disability with or without myoclonic epilepsy
2个月前
已完结
Identification of de novo CSNK2A1 and CSNK2B variants in cases of global developmental delay with seizures
3个月前
已完结
Ultrarapid Nanopore Genome Sequencing in a Critical Care Setting
3个月前
已完结
CSNK2B splice site mutations in patients cause intellectual disability with or without myoclonic epilepsy
3个月前
已完结
[De novo variant of CSNK2B causes Poirier-Bienvenu neurodevelopmental syndrome: two case report]
3个月前
已关闭
CSNK2B splice site mutations in patients cause intellectual disability with or without myoclonic epilepsy
3个月前
已完结
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