(Q33810186)

29 July 2017

Iron overload is rare in patients homozygous for the H63D mutation (English)

1 reference

29 July 2017

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1 reference

Melissa Kelley

1

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29 July 2017

Nikhil Joshi

series ordinal

2

1 reference

29 July 2017

Yagang Xie

series ordinal

3

1 reference

29 July 2017

Mark Borgaonkar

series ordinal

4

1 reference

29 July 2017

language of work or name

English

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publication date

1 April 2014

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Canadian Journal of Gastroenterology & Hepatology

29 July 2017

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29 July 2017

28

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29 July 2017

4

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29 July 2017

198-202

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Creative Commons Attribution-NonCommercial 4.0 International

29 July 2017

start time

1 January 2014

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

1 reference

April 2022 Public Data File from Crossref

cites work

Effects of C282Y, H63D, and S65C HFE gene mutations, diet, and life-style factors on iron status in a general Mediterranean population from Tarragona, Spain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4071918

Iron-overload-related disease in HFE hereditary hemochromatosis

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4071918

Hemochromatosis and iron-overload screening in a racially diverse population.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4071918

Contribution of different HFE genotypes to iron overload disease: a pooled analysis

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4071918

Variable phenotypic presentation of iron overload in H63D homozygotes: are genetic modifiers the cause?

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4071918

Hemochromatosis: diagnosis and management

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4071918

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

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4071918

Genetic screening for HFE hemochromatosis in 6,020 Danish men: penetrance of C282Y, H63D, and S65C variants.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4071918

Hemochromatosis mutations in the general population: iron overload progression rate

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4071918

HFE genotype in patients with hemochromatosis and other liver diseases.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4071918

H63D is an haemochromatosis associated allele

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4071918

Correlation between genotype and phenotype in hereditary hemochromatosis: analysis of 61 cases

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4071918

The significance of the 187G (H63D) mutation in hemochromatosis

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4071918

Prevalence of HFE C282Y and H63D in Jewish populations and clinical implications of H63D homozygosity

30 October 2018

1 reference

12 December 2020

Prevalence and penetrance of HFE mutations in 4865 unselected primary care patients

1 reference

12 December 2020

A genotypic study of 217 unrelated probands diagnosed as "genetic hemochromatosis" on "classical" phenotypic criteria

1 reference

12 December 2020

Individuals homozygous for the H63D mutation have significantly elevated iron indexes

1 reference

12 December 2020

H63D homozygotes with hyperferritinaemia: Is this genotype, the primary cause of iron overload?

1 reference

12 December 2020

Hemochromatosis genotypes and risk of iron overload--a meta-analysis

1 reference

12 December 2020

HFE mutations, iron deficiency and overload in 10,500 blood donors

1 reference

12 December 2020

A population-based study of the biochemical and clinical expression of the H63D hemochromatosis mutation

1 reference

12 December 2020

Identifiers

DOI

10.1155/2014/468521

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29 July 2017

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29 July 2017

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