Evidence for origin, by recurrent mutation, of the phenylalanine hydroxylase R408W mutation on two haplotypes in European and Quebec populations-Reference-Cited by-同舟云学术

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Evidence for origin, by recurrent mutation, of the phenylalanine hydroxylase R408W mutation on two haplotypes in European and Quebec populations

Published:1994 Issue:9 Volume:3 Page:1675-1677
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Hum Mol Genet

Author:

Byck Susan,Morgan Ken,Tyfield Linda,Dworniczak Bernd,Scriver Charles R.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/3/9/1675/1833707/3-9-1675.pdf

Cited by 27 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Phenylketonuria in Portugal: Genotype–phenotype correlations using molecular, biochemical, and haplotypic analyses;Molecular Genetics & Genomic Medicine;2021-01-19

2. A comprehensive study of phenylalanine hydroxylase gene mutations in the Iranian phenylketonuria patients;European Journal of Medical Genetics;2019-09

3. Mutation spectrum of phenylketonuria in Iranian population;Molecular Genetics and Metabolism;2011-01

4. Independent origin of rare Y168H mutation of human phenylalanine hydroxylase gene in Russia;Russian Journal of Genetics;2008-10

5. Persistence of the Common Hartnup Disease D173N Allele in Populations of European Origin;Annals of Human Genetics;2007-11

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