Missense mutations prevalent in orientals with phenylketonuria: Molecular characterization and clinical implications-Reference-Cited by-同舟云学术

Missense mutations prevalent in orientals with phenylketonuria: Molecular characterization and clinical implications

Published:1991-06 Issue:2 Volume:10 Page:449-456
ISSN:0888-7543
Container-title:Genomics
language:en
Short-container-title:Genomics

Author:

Wang Tao,Okano Yoshiyuki,Eisensmith Randy C.,Lo Wilson H.Y.,Huang Shu-Zhen,Zeng Yi-Tao,Yuan Li-Fang,Liu Shen-Ru,Woo Savio L.C.

Publisher

Elsevier BV

Subject

Genetics

Reference45 articles.

1. CpG dinucleotides are mutation hot spots in phenylketonuria;Abadie;Genomics,1989

2. A termination mutation prevalent in Norwegian haplotype 7 phenylketonuria genes;Apold;Am. J. Hum. Genet,1990

3. A single origin of phenylketonuria in Yemenite Jews;Avigad;Nature,1990

4. Polymorphic DNA haplotypes at the human phenylalanine hydroxylase locus and their relationship with phenylketonuria;Chakraborty;Hum. Genet,1987

5. Polymorphic DNA haplotypes at the phenylalanine hydroxylase (PAH) locus in European families with phenylketonuria (PKU);Daiger;Am. J. Hum. Genet,1989

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