Lv1
45 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。
The Biogenesis of Lysosomes
2个月前
已完结
Clinical and genetic analysis of idiopathic intellectual disability/development delay
8个月前
已完结
Docking of Lytic Granules at the Immunological Synapse in Human CTL Requires Vti1b-Dependent Pairing with CD3 Endosomes
9个月前
已完结
Heterozygous de novo variants in HSPD1 cause hypomyelinating leukodystrophy through impaired HSP60 oligomerisation
9个月前
已完结
Rare homozygous nonsense variant in AIMP1 causing Early Onset Epileptic Encephalopathy with Burst Suppression (EOEE-BS)
9个月前
已完结
Ataxia, deafness, leukodystrophy: Inherited disorder of the white matter in three related patients
9个月前
已完结
[Clinical and genetic analysis of a family with Pelizaeus-Merzbacher disease]
10个月前
已关闭
Proteolipid protein 1 gene mutation in nine patients with Pelizaeus-Merzbacher disease
10个月前
已完结
Next-Generation Sequencing in Unexplained Intellectual Disability
10个月前
已完结
Loss-of-function variants inCUL3cause a syndromic neurodevelopmental disorder
11个月前
已完结
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