Lv1
15 积分 2020-03-25 加入
一切我长久喜欢的事物或人，都拥有改变我的力量。
Clinical and genetic analysis of idiopathic intellectual disability/development delay
2个月前
已完结
Docking of Lytic Granules at the Immunological Synapse in Human CTL Requires Vti1b-Dependent Pairing with CD3 Endosomes
3个月前
已完结
Heterozygous de novo variants in HSPD1 cause hypomyelinating leukodystrophy through impaired HSP60 oligomerisation
3个月前
已完结
Rare homozygous nonsense variant in AIMP1 causing Early Onset Epileptic Encephalopathy with Burst Suppression (EOEE-BS)
3个月前
已完结
Ataxia, deafness, leukodystrophy: Inherited disorder of the white matter in three related patients
3个月前
已完结
[Clinical and genetic analysis of a family with Pelizaeus-Merzbacher disease]
4个月前
已关闭
Proteolipid protein 1 gene mutation in nine patients with Pelizaeus-Merzbacher disease
4个月前
已完结
Next-Generation Sequencing in Unexplained Intellectual Disability
4个月前
已完结
Loss-of-function variants inCUL3cause a syndromic neurodevelopmental disorder
5个月前
已完结
OCaR1 endows exocytic vesicles with autoregulatory competence by preventing uncontrolled Ca2+ release, exocytosis, and pancreatic tissue damage
6个月前
已完结
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