Literature DB >> 1358784

Haplotype distribution and mutations at the PAH locus in Croatia.

I Barić1, D Mardesić, G Gjurić, V Sarnavka, B Göbel-Schreiner, U Lichter-Konecki, D S Konecki, F K Trefz.   

Abstract

Restriction fragment length polymorphism (RFLP) haplotypes and mutations at the phenylalanine hydroxylase (PAH) locus have been studied in 25 unrelated families from Croatia. The results of RFLP analysis demonstrated that 80% of the mutant alleles were associated with three haplotypes (1, 2 and 4). Eight mutations were detected on the background of six mutant haplotypes, comprising 68% of phenylketonuria (PKU) alleles in Croatia. The mutation in codon 408 was most frequent, as was the haplotype 2 allele with which it was associated. These data are in accordance with formerly published population genetic analyses at the PAH locus, and with studies revealing the molecular basis of the phenotypic heterogeneity of PKU. The codon 281 mutation was more frequent in Croatia than previously observed in other populations.

Entities:  

Mesh:

Substances:

Year:  1992        PMID: 1358784     DOI: 10.1007/bf00210763

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


  25 in total

1.  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

2.  Phenylalaninaemia. Differential diagnosis.

Authors:  M E Blaskovics; G E Schaeffler; S Hack
Journal:  Arch Dis Child       Date:  1974-11       Impact factor: 3.791

3.  Phenylketonuria missense mutations in the Mediterranean.

Authors:  Y Okano; T Wang; R C Eisensmith; R Longhi; E Riva; M Giovannini; R Cerone; C Romano; S L Woo
Journal:  Genomics       Date:  1991-01       Impact factor: 5.736

4.  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

5.  Molecular basis of phenotypic heterogeneity in phenylketonuria.

Authors:  Y Okano; R C Eisensmith; F Güttler; U Lichter-Konecki; D S Konecki; F K Trefz; M Dasovich; T Wang; K Henriksen; H Lou
Journal:  N Engl J Med       Date:  1991-05-02       Impact factor: 91.245

6.  A prevalent missense mutation in Northern Europe associated with hyperphenylalaninaemia.

Authors:  Y Okano; R C Eisensmith; M Dasovich; T Wang; F Güttler; S L Woo
Journal:  Eur J Pediatr       Date:  1991-03       Impact factor: 3.183

7.  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

8.  Phenylalanine hydroxylase gene: novel missense mutation in exon 7 causing severe phenylketonuria.

Authors:  B Dworniczak; K Grudda; J Stümper; K Bartholomé; C Aulehla-Scholz; J Horst
Journal:  Genomics       Date:  1991-01       Impact factor: 5.736

9.  Genetic analysis of the proximal portion of the mouse t complex: evidence for a second inversion within t haplotypes.

Authors:  B Herrmann; M Bućan; P E Mains; A M Frischauf; L M Silver; H Lehrach
Journal:  Cell       Date:  1986-02-14       Impact factor: 41.582

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

View more
  6 in total

1.  Geographical distribution of the P281L mutation at the phenylalanine hydroxylase locus: possible origin in southeastern Europe.

Authors:  I Barić; D Mardesić; V Sarnavøka; U Lichter-Konecki; D S Konecki; F K Trefz
Journal:  J Inherit Metab Dis       Date:  1994       Impact factor: 4.982

2.  Haplotypes and linkage disequilibrium at the phenylalanine hydroxylase locus, PAH, in a global representation of populations.

Authors:  J R Kidd; A J Pakstis; H Zhao; R B Lu; F E Okonofua; A Odunsi; E Grigorenko; B B Tamir; J Friedlaender; L O Schulz; J Parnas; K K Kidd
Journal:  Am J Hum Genet       Date:  2000-04-27       Impact factor: 11.025

3.  PKU in Slovakia: mutation screening and haplotype analysis.

Authors:  L Kádasi; H Poláková; E Feráková; S Hudecová; T Bohusová; I Szomolayová; J Strnová; I Hruskovic; N K Moschonas; V Ferák
Journal:  Hum Genet       Date:  1995-01       Impact factor: 4.132

4.  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

5.  Preliminary mutation analysis in the phenylalanine hydroxylase gene in Greek PKU and HPA patients.

Authors:  J Traeger-Synodinos; E Kanavakis; M Kalogerakou; K Soulpi; S Missiou-Tsangaraki; C Kattamis
Journal:  Hum Genet       Date:  1994-11       Impact factor: 4.132

6.  Phenylketonuria screening and management in southeastern Europe - survey results from 11 countries.

Authors:  Mojca Zerjav Tansek; Urh Groselj; Natalija Angelkova; Dana Anton; Ivo Baric; Maja Djordjevic; Lindita Grimci; Maria Ivanova; Adil Kadam; Vjosa Kotori; Hajrija Maksic; Oana Marginean; Otilia Margineanu; Olivera Miljanovic; Florentina Moldovanu; Mariana Muresan; Michaela Nanu; Mira Samardzic; Vladimir Sarnavka; Aleksei Savov; Maja Stojiljkovic; Biljana Suzic; Radka Tincheva; Husref Tahirovic; Alma Toromanovic; Natalia Usurelu; Tadej Battelino
Journal:  Orphanet J Rare Dis       Date:  2015-05-30       Impact factor: 4.123

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.