Molecular genetics of phenylketonuria in Orientals: linkage disequilibrium between a termination mutation and haplotype 4 of the phenylalanine hydroxylase gene.

Phenylketonuria (PKU) is a common metabolic disorder among Chinese, with a prevalence of about 1 in 16,500 births. This frequency is very similar to that among Caucasians. Individual exons of the phenylalanine hydroxylase (PAH) gene with flanking introns were amplified by polymerase chain reaction a...

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Bibliografiset tiedot
Päätekijät: Wang, T, Okano, Y, Eisensmith, R, Huang, S Z, Zeng, Y T, Lo, W H, Woo, S L
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 1989
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Research Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC1683443/
https://ncbi.nlm.nih.gov/pubmed/2816939
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