A carregar...

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...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Wang, T, Okano, Y, Eisensmith, R, Huang, S Z, Zeng, Y T, Lo, W H, Woo, S L
Formato: Artigo
Idioma:Inglês
Publicado em: 1989
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1683443/
https://ncbi.nlm.nih.gov/pubmed/2816939
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!