Literature DB >> 1358783

CpG hotspot causes second mutation in codon 408 of the phenylalanine hydroxylase gene.

S J Ramus1, S M Forrest, J A Saleeba, R G Cotton.   

Abstract

A new mutation has been identified in exon 12 of the gene encoding phenylalanine hydroxylase at codon 408. The single base change from guanine to adenine changes the amino acid arginine to glutamine; thus, the mutation is defined as R408Q. This codon is the site of a mutation known to causes phenylketonuria. Both these mutations are located at the same CpG site.

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Year:  1992        PMID: 1358783     DOI: 10.1007/bf00210760

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  11 in total

1.  Missense mutations prevalent in Orientals with phenylketonuria: molecular characterization and clinical implications.

Authors:  T Wang; Y Okano; R C Eisensmith; W H Lo; S Z Huang; Y T Zeng; L F Yuan; S R Liu; S L Woo
Journal:  Genomics       Date:  1991-06       Impact factor: 5.736

2.  A simple salting out procedure for extracting DNA from human nucleated cells.

Authors:  S A Miller; D D Dykes; H F Polesky
Journal:  Nucleic Acids Res       Date:  1988-02-11       Impact factor: 16.971

3.  Improvement of PCR amplified DNA sequencing with the aid of detergents.

Authors:  B Bachmann; W Lüke; G Hunsmann
Journal:  Nucleic Acids Res       Date:  1990-03-11       Impact factor: 16.971

4.  CpG dinucleotides are mutation hot spots in phenylketonuria.

Authors:  V Abadie; S Lyonnet; N Maurin; M Berthelon; C Caillaud; F Giraud; J F Mattei; J Rey; F Rey; A Munnich
Journal:  Genomics       Date:  1989-11       Impact factor: 5.736

5.  Molecular basis of base substitution hotspots in Escherichia coli.

Authors:  C Coulondre; J H Miller; P J Farabaugh; W Gilbert
Journal:  Nature       Date:  1978-08-24       Impact factor: 49.962

Review 6.  Phenylketonuria and other phenylalanine hydroxylation mutants in man.

Authors:  C R Scriver; C L Clow
Journal:  Annu Rev Genet       Date:  1980       Impact factor: 16.830

7.  Tight linkage between a splicing mutation and a specific DNA haplotype in phenylketonuria.

Authors:  A G DiLella; J Marvit; A S Lidsky; F Güttler; S L Woo
Journal:  Nature       Date:  1986 Aug 28-Sep 3       Impact factor: 49.962

8.  An amino-acid substitution involved in phenylketonuria is in linkage disequilibrium with DNA haplotype 2.

Authors:  A G DiLella; J Marvit; K Brayton; S L Woo
Journal:  Nature       Date:  1987 May 28-Jun 3       Impact factor: 49.962

9.  Screening for phenylketonuria mutations by DNA amplification with the polymerase chain reaction.

Authors:  A G DiLella; W M Huang; S L Woo
Journal:  Lancet       Date:  1988-03-05       Impact factor: 79.321

10.  Missense mutations associated with RFLP haplotypes 1 and 4 of the human phenylalanine hydroxylase gene.

Authors:  Y Okano; T Wang; R C Eisensmith; B Steinmann; R Gitzelmann; S L Woo
Journal:  Am J Hum Genet       Date:  1990-01       Impact factor: 11.025

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  1 in total

1.  Recurrence of the R408W mutation in the phenylalanine hydroxylase locus in Europeans.

Authors:  R C Eisensmith; A A Goltsov; C O'Neill; L A Tyfield; E I Schwartz; A I Kuzmin; S S Baranovskaya; G L Tsukerman; E Treacy; C R Scriver
Journal:  Am J Hum Genet       Date:  1995-01       Impact factor: 11.025

  1 in total

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