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10 积分 2022-01-18 加入
Phenylalanine hydroxylase genotype-phenotype associations in the United States: A single center study
7个月前
已完结
Phenylalanine hydroxylase genotype-phenotype associations in the United States: A single center study
7个月前
已完结
The molecular basis of phenylketonuria in Koreans
7个月前
已完结
Molecular characterization of phenylketonuria in Japanese patients
7个月前
已完结
Molecular characterization of phenylketonuria and tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency in Japan
7个月前
已完结
Mutations of the phenylalanine hydroxylase (PAH) gene in Brazilian patients with phenylketonuria
7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
7个月前
已完结
PREVALENCE OF PAH MUTATIONS IN GEORGIAN PKU PATIENTS COMPARED TO MOST FREQUENT PAH MUTATIONS IN EUROPEAN POPULATIONS
7个月前
已关闭
Phenylketonuria mutations in Europe
7个月前
已完结
Mutational and phenotypical spectrum of phenylalanine hydroxylase deficiency in Denmark
7个月前
已完结
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