Lv1
38 积分 2024-12-02 加入
A clinical variance in familial amyotrophic lateral sclerosis with a point mutation in Cu/Zn superoxide dismutase gene
1个月前
已完结
Mutations in the reverse transcriptase component of telomerase (TERT) in patients with bone marrow failure
1个月前
已完结
A study of the SCN5A gene in a cohort of 76 patients with Brugada syndrome
1个月前
已完结
Analysis of genetic variant in a child with autosomal recessive Alport syndrome
2个月前
已完结
Molecular epidemiology of spinocerebellar ataxias in Cuba: Insights into SCA2 founder effect in Holguin
6个月前
已完结
The identification of novel mutations in the biotinidase gene using denaturing high pressure liquid chromatography (dHPLC)
6个月前
已完结
FSIP2plays a role in the acrosome development during spermiogenesis
6个月前
已完结
[Clinical phenotype and gene analysis of 86 cases of 5 alpha reductase deficiency]
7个月前
已完结