Literature DB >> 2896155

Linkage disequilibrium between RFLP haplotype 2 and the affected PAH allele in PKU families from the Berlin area of the German Democratic Republic.

O Riess1, A Michel, A Speer, W Meiske, G Cobet, C Coutelle.   

Abstract

Probands from 26 PKU-affected families of the Berlin area were analyzed with respect to the allele frequency distribution of six RFLPs in linkage with the normal and the PKU alleles of the phenylalanine hydroxylase gene. These investigations confirm most of the RFLP haplotypes observed by Güttler and colleagues in the Danish population and describe two additional ones. They detect no significant differences in the single RFLP or RFLP haplotype distribution on the normal chromosomes in comparison with the Danish families and confirm a prevalent association of the RFLP haplotypes 1, 4, and 7 with the normal PAH allele. In contrast to the Danish investigations, in our study the PKU allele is found most frequently linked to haplotype 2, rather then to haplotype 3. In one of our patients we found a substitution of the normal 19-kb MspI fragment by a 13.5- and a 5.5-kb fragment, reported up to now only in one other German family.

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Year:  1988        PMID: 2896155     DOI: 10.1007/bf00291732

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


  8 in total

1.  Recurrent mutations in haemophilia A give evidence for CpG mutation hotspots.

Authors:  H Youssoufian; H H Kazazian; D G Phillips; S Aronis; G Tsiftis; V A Brown; S E Antonarakis
Journal:  Nature       Date:  1986 Nov 27-Dec 3       Impact factor: 49.962

2.  Extensive restriction site polymorphism at the human phenylalanine hydroxylase locus and application in prenatal diagnosis of phenylketonuria.

Authors:  A S Lidsky; F D Ledley; A G DiLella; S C Kwok; S P Daiger; K J Robson; S L Woo
Journal:  Am J Hum Genet       Date:  1985-07       Impact factor: 11.025

3.  Molecular genetics of PKU.

Authors:  F Güttler; S L Woo
Journal:  J Inherit Metab Dis       Date:  1986       Impact factor: 4.982

4.  Typing of families with classical phenylketonuria using three alleles of the Hindiii linked restriction fragment polymorphism, detectable with a phenylalanine hydroxylase cDNA probe. Family typing for PKU by linked HindIII RFLP.

Authors:  A Speer; H H Dahl; O Riess; G Cobet; R Hanke; R G Cotton; C Coutelle
Journal:  Clin Genet       Date:  1986-06       Impact factor: 4.438

5.  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

6.  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

7.  Polymorphic DNA haplotypes at the human phenylalanine hydroxylase locus and their relationship with phenylketonuria.

Authors:  R Chakraborty; A S Lidsky; S P Daiger; F Güttler; S Sullivan; A G Dilella; S L Woo
Journal:  Hum Genet       Date:  1987-05       Impact factor: 4.132

8.  Molecular analysis of the inheritance of phenylketonuria and mild hyperphenylalaninemia in families with both disorders.

Authors:  F D Ledley; H L Levy; S L Woo
Journal:  N Engl J Med       Date:  1986-05-15       Impact factor: 91.245

  8 in total
  19 in total

1.  Linkage disequilibrium between phenylketonuria and RFLP haplotype 1 at the phenylalanine hydroxylase locus in Portugal.

Authors:  C Caillaud; L Vilarinho; A Vilarinho; F Rey; M Berthelon; R Santos; S Lyonnet; M L Briard; R V Osorio; J Rey
Journal:  Hum Genet       Date:  1992-04       Impact factor: 4.132

Review 2.  Heterogeneity of phenylketonuria at the clinical, protein and DNA levels.

Authors:  R G Cotton
Journal:  J Inherit Metab Dis       Date:  1990       Impact factor: 4.982

3.  Molecular heterogeneity at the phenylalanine hydroxylase locus in the population of the south-west of England.

Authors:  L A Tyfield; M J Osborn; J B Holton
Journal:  J Med Genet       Date:  1991-04       Impact factor: 6.318

4.  Identification of the haplotype pattern associated with the mutant PKU allele in the Gypsy population of Wales.

Authors:  L A Tyfield; A L Meredith; M J Osborn; P S Harper
Journal:  J Med Genet       Date:  1989-08       Impact factor: 6.318

5.  DNA haplotype analyses of patients with hyperphenylalaninemia.

Authors:  D Di Silvestre; A Pandya; R Koch; J Groffen
Journal:  Am J Hum Genet       Date:  1990-10       Impact factor: 11.025

Review 6.  The phenylketonuria locus: current knowledge about alleles and mutations of the phenylalanine hydroxylase gene in various populations.

Authors:  D S Konecki; U Lichter-Konecki
Journal:  Hum Genet       Date:  1991-08       Impact factor: 4.132

7.  Molecular analysis of PKU haplotypes in the population of southern Poland.

Authors:  M Zygulska; A Eigel; C Aulehla-Scholz; J J Pietrzyk; J Horst
Journal:  Hum Genet       Date:  1991-01       Impact factor: 4.132

8.  Geographical distribution gradients of the major PKU mutations and the linked haplotypes.

Authors:  L Kalaydjieva; B Dworniczak; V Kucinskas; V Yurgeliavicius; E Kunert; J Horst
Journal:  Hum Genet       Date:  1991-02       Impact factor: 4.132

9.  The identification of two mis-sense mutations at the PAH gene locus in a Turkish patient with phenylketonuria.

Authors:  D S Konecki; M Schlotter; F K Trefz; U Lichter-Konecki
Journal:  Hum Genet       Date:  1991-08       Impact factor: 4.132

10.  The codon 408 mutation associated with haplotype 2 is predominant in Polish families with phenylketonuria.

Authors:  J Jaruzelska; K F Henriksen; F Güttler; O Riess; K Borski; N Blin; R Slomski
Journal:  Hum Genet       Date:  1991-01       Impact factor: 4.132

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