Literature DB >> 11680538

The frequency of C282Y and H63D mutations in Hemochromatosis gene in native Estonians.

P Pärlist1, A V Mikelsaar, G Tasa, L Beckman.   

Abstract

Four hundred and forty two adult individuals of Estonian nationality were examined in different regions of Estonia for the C282Y and H63D HFE mutations to determine the allele and genotype frequencies. The sample consisted only of those people whose at least four grandparents were born in Estonia, and have lived settled in the same region. The study was carried out using the PCR technique and restriction analysis for C282Y and H63D mutations respectively. For the C282Y mutation the frequency of heterozygotes was 6.6% and homozygotes 0.2%, giving allele frequency 0.035. The allele frequency for the H63D mutation was 0.136, and the frequency of homo- and hetero-zygotes 1.6% and 24.0% respectively.

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Year:  2001        PMID: 11680538     DOI: 10.1023/a:1017951314164

Source DB:  PubMed          Journal:  Eur J Epidemiol        ISSN: 0393-2990            Impact factor:   8.082


  11 in total

1.  Global prevalence of putative haemochromatosis mutations.

Authors:  A T Merryweather-Clarke; J J Pointon; J D Shearman; K J Robson
Journal:  J Med Genet       Date:  1997-04       Impact factor: 6.318

2.  A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis.

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Journal:  Nat Genet       Date:  1996-08       Impact factor: 38.330

3.  Prevalence of hemochromatosis among 11,065 presumably healthy blood donors.

Authors:  C Q Edwards; L M Griffen; D Goldgar; C Drummond; M H Skolnick; J P Kushner
Journal:  N Engl J Med       Date:  1988-05-26       Impact factor: 91.245

Review 4.  Prevalence of hereditary hemochromatosis in a Massachusetts corporation: is Celtic origin a risk factor?

Authors:  B N Smith; W Kantrowitz; N D Grace; M S Greenberg; T J Patton; R Ookubo; K Sorger; J G Semeraro; J R Doyle; A G Cooper; B R Kamat; L M Maregni; W M Rand
Journal:  Hepatology       Date:  1997-06       Impact factor: 17.425

5.  Haplotype analysis of hemochromatosis: evaluation of different linkage-disequilibrium approaches and evolution of disease chromosomes.

Authors:  R S Ajioka; L B Jorde; J R Gruen; P Yu; D Dimitrova; J Barrow; E Radisky; C Q Edwards; L M Griffen; J P Kushner
Journal:  Am J Hum Genet       Date:  1997-06       Impact factor: 11.025

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Authors:  M Simon; J L Alexandre; R Fauchet; B Genetet; M Bourel
Journal:  Prog Med Genet       Date:  1980

7.  Ethnic differences in the HFE codon 282 (Cys/Tyr) polymorphism.

Authors:  L E Beckman; N Saha; V Spitsyn; G Van Landeghem; L Beckman
Journal:  Hum Hered       Date:  1997 Sep-Oct       Impact factor: 0.444

Review 8.  Hemochromatosis: a genetic defect in iron metabolism.

Authors:  E C Jazwinska
Journal:  Bioessays       Date:  1998-07       Impact factor: 4.345

9.  Hereditary hemochromatosis. Phenotypic expression of the disease.

Authors:  G E Cartwright; C Q Edwards; K Kravitz; M Skolnick; D B Amos; A Johnson; L Buskjaer
Journal:  N Engl J Med       Date:  1979-07-26       Impact factor: 91.245

10.  Celtic origin of the C282Y mutation of hemochromatosis.

Authors:  G Lucotte
Journal:  Blood Cells Mol Dis       Date:  1998-12       Impact factor: 3.039

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  1 in total

1.  Prevalence of 845G>A HFE mutation in Slavic populations: an east-west linear gradient in South Slavs.

Authors:  Grazyna Adler; Jeremy S Clark; Beata Łoniewska; Andrzej Ciechanowicz
Journal:  Croat Med J       Date:  2011-06       Impact factor: 1.351

  1 in total

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