Lv1
50 积分 2022-10-21 加入
DNAJC13 p.Asn855Ser, implicated in familial parkinsonism, alters membrane dynamics of sorting nexin 1
15天前
已完结
Biallelic SHQ1 variants in early infantile hypotonia and paroxysmal dystonia as the leading manifestation
2个月前
已完结
Compound heterozygous mutation of AFG3L2 causes autosomal recessive spinocerebellar ataxia through mitochondrial impairment and MICU1 mediated Ca2+ overload
2个月前
已完结
Huntingtin-deficient zebrafish exhibit defects in iron utilization and development
3个月前
已完结
Variants in CSMD2 and CSMD3, genes involved in synaptogenesis, are associated with epilepsies
4个月前
已完结
Protein palmitoylation activate zygotic gene expression during the maternal-to-zygotic transition
5个月前
已完结
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