Lv1
10 积分 2022-11-07 加入
SARS1 (SerRS) Causing De Novo Dominant Charcot–Marie–Tooth Disease with Slow Conduction
2天前
已完结
Biomimetic Nano‐Immunoactivator via Ionic Metabolic Modulation for Strengthened NIR‐II Photothermal Immunotherapy
9个月前
已完结
Disease‐associated missense variants in ZBTB18 disrupt DNA binding and impair the development of neurons within the embryonic cerebral cortex
11个月前
已完结
A novel heterozygous ZBTB18 missense mutation in a family with non-syndromic intellectual disability
11个月前
已完结
MYO1H is a novel candidate gene for autosomal dominant pure hereditary spastic paraplegia
1年前
已完结
A founder mutation in COQ7, p.(Leu111Pro), causes pure hereditary spastic paraplegia (HSP) in the Iranian population
1年前
已完结
A novel ATP13A2 variant causing complicated hereditary spastic paraplegia
1年前
已完结
Diverse CMT2 neuropathies are linked to aberrant G3BP interactions in stress granules
1年前
已完结
Relative Contribution of Genetic and Environmental Factors in CKD
1年前
已关闭
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