Lv1
50 积分 2022-10-21 加入
Biallelic SHQ1 variants in early infantile hypotonia and paroxysmal dystonia as the leading manifestation
8天前
已完结
Compound heterozygous mutation of AFG3L2 causes autosomal recessive spinocerebellar ataxia through mitochondrial impairment and MICU1 mediated Ca2+ overload
10天前
已完结
Huntingtin-deficient zebrafish exhibit defects in iron utilization and development
1个月前
已完结
Variants in CSMD2 and CSMD3, genes involved in synaptogenesis, are associated with epilepsies
2个月前
已完结
Protein palmitoylation activate zygotic gene expression during the maternal-to-zygotic transition
3个月前
已完结
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