Lv5
979 积分 2024-11-14 加入
[Analysis of SPTA1 gene mutations in a patient with hereditary elliptocytosis]
1年前
已完结
Two novel glucose 6-phosphate dehydrogenase deficiency mutations and association of such mutations with F8C/G6PD haplotype in Chinese
1年前
已关闭
Glucose-6-phosphate dehydrogenase mutations in Mon and Burmese of southern Myanmar
1年前
已完结
High mutation rate of NPHP3 in 18 Chinese infantile nephronophthisis patients
1年前
已完结
Diagnostic and clinical utility of genetic testing in children with kidney failure
1年前
已完结
Diagnostic and clinical utility of genetic testing in children with kidney failure
1年前
已完结
Mutation analysis and characterization of alternative splice variants of the Wilson disease gene ATP7B
1年前
已完结
Six novel ATP7B mutations in Thai patients with Wilson disease
1年前
已完结
Distinct clinical courses according to presenting phenotypes and their correlations to ATP7B mutations in a large Wilson's disease cohort
1年前
已完结
Mutation analysis of 73 southern Chinese Wilson's disease patients: identification of 10 novel mutations and its clinical correlation
1年前
已完结
皖公网安备34019202002308
