The phenylketonuria G272X haplotype 7 mutation in European populations-Reference-Cited by-同舟云学术

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The phenylketonuria G272X haplotype 7 mutation in European populations

Published:1993-09 Issue:2 Volume:92 Page:
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Apold Jaran,Eiken HansG.,Svensson Elisabeth,Kunert Erich,Kozak Libor,Cechak Petr,G�ttler Flemming,Giltay Jacques,Lichter-Konecki Uta,Melle Dominique,Jaruzelska JadwigaMaria

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF00219674.pdf

Cited by 6 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 mutations in Europe;Human Mutation;2003-03-19

2. Phenylalanine hydroxylase genotypes, predicted residual enzyme activity and phenotypic parameters of diagnosis and treatment of phenylketonuria;European Journal of Pediatrics;1996-01

3. PKU mutation G46S is associated with increased aggregation and degradation of the phenylalanine hydroxylase enzyme;Human Mutation;1996

4. 6 Molecular Genetics of Phenylketonuria: From Molecular Anthropology to Gene Therapy;Advances in Genetics;1995

5. Population genetics of phenylketonuria;Acta Paediatrica;1994-12

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