Literature DB >> 11757579

Mutation analysis in Turkish patients with hereditary fructose intolerance.

A Dursun1, H S Kalkanoğlu, T Coşkun, A Tokatli, R Bittner, N Koçak, A Yüce, I Ozalp, H J Boehme.   

Abstract

Thirteen Turkish patients with hereditary fructose intolerance (HFI) were screened for the three common mutations, A149P, A174D and N334K, in the aldolase B gene that have been detected frequently in European population. We found that nine of the patients carry the A149P mutation in both alleles, which corresponds to a frequency of about 55%. Single-strand conformation analysis of all coding exons of the gene was also performed to detect unknown mutations in four patients not carrying the three common mutations. No aberrant migration patterns were observed in these patients.

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Year:  2001        PMID: 11757579     DOI: 10.1023/a:1012423624993

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


  7 in total

1.  Expression, purification, and characterization of natural mutants of human aldolase B. Role of quaternary structure in catalysis.

Authors:  P Rellos; J Sygusch; T M Cox
Journal:  J Biol Chem       Date:  2000-01-14       Impact factor: 5.157

2.  Association of the widespread A149P hereditary fructose intolerance mutation with newly identified sequence polymorphisms in the aldolase B gene.

Authors:  C C Brooks; D R Tolan
Journal:  Am J Hum Genet       Date:  1993-04       Impact factor: 11.025

3.  Complete amino acid sequence for human aldolase B derived from cDNA and genomic clones.

Authors:  W H Rottmann; D R Tolan; E E Penhoet
Journal:  Proc Natl Acad Sci U S A       Date:  1984-05       Impact factor: 11.205

4.  Characterization of the human aldolase B gene.

Authors:  D R Tolan; E E Penhoet
Journal:  Mol Biol Med       Date:  1986-06

5.  Null alleles of the aldolase B gene in patients with hereditary fructose intolerance.

Authors:  M Ali; G Tunçman; N C Cross; M Vidailhet; I Bökesoy; R Gitzelmann; T M Cox
Journal:  J Med Genet       Date:  1994-06       Impact factor: 6.318

6.  Catalytic deficiency of human aldolase B in hereditary fructose intolerance caused by a common missense mutation.

Authors:  N C Cross; D R Tolan; T M Cox
Journal:  Cell       Date:  1988-06-17       Impact factor: 41.582

7.  Molecular analysis of aldolase B genes in hereditary fructose intolerance.

Authors:  N C Cross; R de Franchis; G Sebastio; C Dazzo; D R Tolan; C Gregori; M Odievre; M Vidailhet; V Romano; G Mascali
Journal:  Lancet       Date:  1990-02-10       Impact factor: 79.321

  7 in total
  1 in total

1.  Increased prevalence of mutant null alleles that cause hereditary fructose intolerance in the American population.

Authors:  Erin M Coffee; Laura Yerkes; Elizabeth P Ewen; Tiffany Zee; Dean R Tolan
Journal:  J Inherit Metab Dis       Date:  2009-12-23       Impact factor: 4.982

  1 in total

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