Phenylalanine hydroxylase gene: silent mutation uncovers evolutionary origin of different alleles-Reference-Cited by-同舟云学术

Phenylalanine hydroxylase gene: silent mutation uncovers evolutionary origin of different alleles

Published:2008-06-28 Issue:4 Volume:38 Page:270-273
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Dworniczak Bernd,Aulehla-Scholz Christa,Horst Jürgen

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1990.tb03580.x/fullpdf

Reference6 articles.

1. Phenylketonuria: distribution of DNA diagnostic patterns in German families;Aulehla-Scholz;Hum. Genet.,1988

2. The CpG dinucleotide and human genetic disease;Cooper;Hum. Genet.,1988

3. Nucleotide sequence of a full-length complementary DNA clone and amino acid sequence of human phenylalanine hydroxylase;Kwok;Biochemistry,1985

4. Extensive restriction site polymorphism at the human phenylalanine hydroxylase locus and application in prenatal diagnosis of phenylketonuria;Lidsky;Am. J. Hum. Genet.,1985

5. Meiotic recombination between two polymorphic restriction sites within the β globin gene cluster;Old;J. Med. Genet.,1986

Cited by 7 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. Selection for Translation Efficiency on Synonymous Polymorphisms in Recent Human Evolution;Genome Biology and Evolution;2011-01-01

2. Phenylketonuria mutations and their relation to RFLP haplotypes at the PAH locus in Czech PKU families;Human Genetics;1995-10

3. Mutations Ivs4nt1, 47delCT, and G148S identified in the phenylalanine hydroxylase gene by RT-PCR of illegitimate transcripts and chemical cleavage of mismatch;Human Mutation;1995

4. Analysis of exon 7 of the human phenylalanine hydroxylase gene: A mutation hot spot?;Human Mutation;1992

5. Molecular basis of phenylketonuria and related hyperphenylalaninemias: Mutations and polymorphisms in the human phenylalanine hydroxylase gene;Human Mutation;1992