Identification of ferroportin disease in the Indian subcontinent. (Q42578607)

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9 January 2020

title

Identification of ferroportin disease in the Indian subcontinent (English)

1 reference

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9 January 2020

0 references

1

1 reference

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9 January 2020

Nathan V Subramaniam

6

1 reference

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9 January 2020

author name string

P Browett

2

1 reference

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9 January 2020

P Wong

3

1 reference

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9 January 2020

H Kua

4

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9 January 2020

R Ameratunga

5

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language of work or name

English

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publication date

1 April 2005

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9 January 2020

1 reference

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9 January 2020

volume

54

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9 January 2020

issue

4

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9 January 2020

page(s)

567-568

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9 January 2020

cites work

The ferroportin disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1774468

A valine deletion of ferroportin 1: a common mutation in hemochromastosis type 4

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1774468

Autosomal dominant reticuloendothelial iron overload associated with a 3-base pair deletion in the ferroportin 1 gene (SLC11A3)

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1774468

Novel mutation in ferroportin1 is associated with autosomal dominant hemochromatosis

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1774468

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

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1774468

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

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1774468

Genetic hyperferritinaemia and reticuloendothelial iron overload associated with a three base pair deletion in the coding region of the ferroportin gene (SLC11A3).

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1774468

Distribution of C282Y and H63D mutations in the HFE gene in healthy Asian Indians and patients with thalassaemia major

16 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15753550

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Non-HFE hemochromatosis

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15753550

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/GUT.2004.060988

1 reference

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9 January 2020

1 reference

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9 January 2020

1 reference

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