(Q34224747)

31 July 2017

title

Frequency of primary iron overload and HFE gene mutations (C282Y, H63D and S65C) in chronic liver disease patients in north India (English)

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31 July 2017

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chronic liver disease

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inferred from title

author name string

Barjinderjit Kaur Dhillon

1

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31 July 2017

Reena Das

2

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31 July 2017

Gurjeewan Garewal

3

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31 July 2017

Yogesh Chawla

4

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31 July 2017

R K Dhiman

5

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31 July 2017

Ashim Das

6

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31 July 2017

Ajay Duseja

7

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31 July 2017

G R Chandak

8

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31 July 2017

language of work or name

English

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publication date

1 June 2007

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World Journal of Gastroenterology

31 July 2017

published in

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31 July 2017

volume

13

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31 July 2017

issue

21

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31 July 2017

page(s)

2956-2959

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Nonalcoholic steatohepatitis in Asian Indians is neither associated with iron overload nor with HFE gene mutations

31 July 2017

cites work

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4171148

The effect of HFE genotypes on measurements of iron overload in patients attending a health appraisal clinic

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4171148

Global prevalence of putative haemochromatosis mutations

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4171148

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4171148

Liver pathology in genetic hemochromatosis: a review of 135 homozygous cases and their bioclinical correlations

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4171148

Absence of hemochromatosis associated Cys282Tyr HFE gene mutation and low frequency of hemochromatosis phenotype in nonalcoholic chronic liver disease patients in India.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4171148

The C282Y mutation of the HFE gene is not found in Chinese haemochromatotic patients: multicentre retrospective study

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4171148

HFE genotype in patients with hemochromatosis and other liver diseases.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4171148

Genotypic/phenotypic correlations in genetic hemochromatosis: evolution of diagnostic criteria.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4171148

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

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4171148

Genetic and clinical description of hemochromatosis probands and heterozygotes: evidence that multiple genes linked to the major histocompatibility complex are responsible for hemochromatosis

28 October 2018

1 reference

12 December 2020

HFE mutations analysis in 711 hemochromatosis probands: evidence for S65C implication in mild form of hemochromatosis

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12 December 2020

Frequencies in the Japanese population of HFE gene mutations

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12 December 2020

Prevalence of the H63D mutation of the HFE in north India: its presence does not cause iron overload in beta thalassemia trait

1 reference

12 December 2020

Long-term survival in patients with hereditary hemochromatosis

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12 December 2020

HFE, hepcidin and ferroportin gene mutations are not present in Indian patients with primary haemochromatosis

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12 December 2020

A Chinese patient with non-HFE-linked iron overload

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12 December 2020

Identifiers

DOI

10.3748/WJG.V13.I21.2956

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31 July 2017

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31 July 2017

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