Lv7
4990 积分 2021-01-07 加入
GATORopathies: The role of amino acid regulatory gene mutations in epilepsy and cortical malformations
21小时前
已完结
Identification of the minimal combination of clinical features in probands for efficient mutation detection in the FBN1 gene
2个月前
已完结
Identification of the minimal combination of clinical features in probands for efficient mutation detection in the FBN1 gene
2个月前
已完结
Cytochrome P450 2U1, a very peculiar member of the human P450s family
9个月前
已完结
Mutation profile and treatment of Gitelman syndrome in Chinese patients
9个月前
已完结
R158Q and G212S, novel pathogenic compound heterozygous variants in SLC12A3 of Gitelman syndrome
9个月前
已完结
Systematic Intravenous Administration of Autologous Mesenchymal Stem Cells Is Safe
1年前
已完结
AAV9-Mediated Gene Therapy for Infantile-Onset Pompe’s Disease
1年前
已完结
[Alpha-galactosidase A gene mutation in a Chinese family with Fabry disease mimicking clinical features of hypertrophic cardiomyopathy]
1年前
已关闭
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