Literature DB >> 8105144

Haplotype distribution at the phenylalanine hydroxylase locus in PKU families from the Moravian area of Czechoslovakia.

L Kozák1, D Dvoráková, A Pijácková, J Kamarýt.   

Abstract

The analysis of 21 families affected with classical phenylketonuria (PKU) from the Moravian area of Czechoslovakia has revealed 12 different RFLP haplotypes. Nine and eight haplotypes were associated with the normal and with the mutant alleles, respectively. Most normal alleles are associated with haplotype 1 (42.9%). Almost 80% of all mutant alleles are confined within only three haplotypes (1, 2 and 4). There was a strong association between haplotype 2 and the Czech mutant alleles (61.9% of the mutant alleles compared with 4.8% of the normal alleles). There was linkage disequilibrium between this haplotype and the R408W mutation in exon 12. Two mutant haplotypes 7 were found and in both cases they were tightly linked with G272ter mutation. Our finding is in agreement with observations in other Eastern European countries. These data provide further support for the theories of the spread of the R408W mutation from east to west in European populations.

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Year:  1993        PMID: 8105144     DOI: 10.1007/bf00710297

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  25 in total

1.  Clinical and molecular heterogeneity of phenylalanine hydroxylase deficiencies in France.

Authors:  F Rey; M Berthelon; C Caillaud; S Lyonnet; V Abadie; F Blandin-Savoja; J Feingold; J M Saudubray; J Frézal; A Munnich
Journal:  Am J Hum Genet       Date:  1988-12       Impact factor: 11.025

2.  Nucleotide sequence of a full-length complementary DNA clone and amino acid sequence of human phenylalanine hydroxylase.

Authors:  S C Kwok; F D Ledley; A G DiLella; K J Robson; S L Woo
Journal:  Biochemistry       Date:  1985-01-29       Impact factor: 3.162

3.  Two distinct mutations at a single BamHI site in phenylketonuria.

Authors:  D Melle; P Verelst; F Rey; M Berthelon; B François; A Munnich; S Lyonnet
Journal:  J Med Genet       Date:  1991-01       Impact factor: 6.318

4.  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

5.  Polymorphic DNA haplotypes at the phenylalanine hydroxylase locus and their relation to phenotype in Swedish phenylketonuria families.

Authors:  E Svensson; U von Döbeln; L Hagenfeldt
Journal:  Hum Genet       Date:  1991-05       Impact factor: 4.132

6.  DNA haplotype analysis at the phenylalanine hydroxylase locus in the Turkish population.

Authors:  U Lichter-Konecki; M Schlotter; C Yaylak; M Ozgüç; T Coskun; I Ozalp; U Wendel; U Batzler; F K Trefz; D Konecki
Journal:  Hum Genet       Date:  1989-03       Impact factor: 4.132

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.  Application of natural and amplification created restriction sites for the diagnosis of PKU mutations.

Authors:  H G Eiken; E Odland; H Boman; L Skjelkvåle; L F Engebretsen; J Apold
Journal:  Nucleic Acids Res       Date:  1991-04-11       Impact factor: 16.971

9.  Haplotype distribution and molecular defects at the phenylalanine hydroxylase locus in Italy.

Authors:  I Dianzani; M Devoto; C Camaschella; G Saglio; G B Ferrero; R Cerone; C Romano; G Romeo; M Giovannini; E Riva
Journal:  Hum Genet       Date:  1990-11       Impact factor: 4.132

10.  Two mutations within the coding sequence of the phenylalanine hydroxylase gene.

Authors:  E Svensson; B Andersson; L Hagenfeldt
Journal:  Hum Genet       Date:  1990-08       Impact factor: 4.132

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  2 in total

1.  Mutation and haplotype analysis of phenylalanine hydroxylase alleles in classical PKU patients from the Czech Republic: identification of four novel mutations.

Authors:  L Kozák; M Blazková; V Kuhrová; A Pijácková; S Růzicková; S St'astná
Journal:  J Med Genet       Date:  1997-11       Impact factor: 6.318

2.  Phenylketonuria mutations and their relation to RFLP haplotypes at the PAH locus in Czech PKU families.

Authors:  L Kozák; V Kuhrová; M Blazková; V Romano; L Fajkusová; D Dvoráková; A Pijácková
Journal:  Hum Genet       Date:  1995-10       Impact factor: 4.132

  2 in total

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