Spectrum of phenylketonuria mutations in Western Europe and North Africa, and their relation to polymorphic DNA haplotypes at the phenylalanine hydroxylase locus-Reference-Cited by-同舟云学术

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Spectrum of phenylketonuria mutations in Western Europe and North Africa, and their relation to polymorphic DNA haplotypes at the phenylalanine hydroxylase locus

Published:1991-02 Issue:4 Volume:86 Page:355-358
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Berthelon Monique,Caillaud Catherine,Rey Françoise,Labrune Philippe,Melle Dominique,Feingold Josué,Frézal Jean,Briard Marie-Louise,Farriaux Jean-Pierre,Guibaud Pierre,Journel Hubert,Le Marec Bernard,Maurin Nicole,Nivelon Jean-Louis,Plauchu Henri,Saudubray Jean-Marie,Tron Philippe,Rey Jean,Münnich Arnold,Lyonnet Stanislas

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF00201832.pdf

Cited by 22 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. A novel 22bp deletion in a Tunisian phenylketonuria family;Pathologie Biologie;2012-12

4. Screening of three Mediterranean phenylketonuria mutations in Tunisian families;Journal of Genetics;2012-04

5. Introduction: Genetic Diversity Among Arabs;Genetic Disorders Among Arab Populations;2010

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