Lv1
10 积分 2022-01-18 加入
Phenylalanine hydroxylase genotype-phenotype associations in the United States: A single center study
9个月前
已完结
Phenylalanine hydroxylase genotype-phenotype associations in the United States: A single center study
9个月前
已完结
The molecular basis of phenylketonuria in Koreans
9个月前
已完结
Molecular characterization of phenylketonuria in Japanese patients
9个月前
已完结
Molecular characterization of phenylketonuria and tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency in Japan
9个月前
已完结
Mutations of the phenylalanine hydroxylase (PAH) gene in Brazilian patients with phenylketonuria
10个月前
已完结
Mutation analysis of PAH gene in patients with PKU in western Iran and its association with polymorphisms: identification of four novel mutations
10个月前
已完结
PREVALENCE OF PAH MUTATIONS IN GEORGIAN PKU PATIENTS COMPARED TO MOST FREQUENT PAH MUTATIONS IN EUROPEAN POPULATIONS
10个月前
已关闭
Phenylketonuria mutations in Europe
10个月前
已完结
Mutational and phenotypical spectrum of phenylalanine hydroxylase deficiency in Denmark
10个月前
已完结
皖公网安备34019202002308
