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English
Identification of ferroportin disease in the Indian subcontinent.
scientific article published on April 2005
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
1774468
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15753550%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 January 2020
title
Identification of ferroportin disease in the Indian subcontinent
(English)
1 reference
stated in
Europe PubMed Central
PMCID
1774468
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15753550%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 January 2020
main subject
India
0 references
author
Daniel F. Wallace
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
1774468
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15753550%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 January 2020
Nathan V Subramaniam
series ordinal
6
1 reference
stated in
Europe PubMed Central
PMCID
1774468
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15753550%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 January 2020
author name string
P Browett
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMCID
1774468
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15753550%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 January 2020
P Wong
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMCID
1774468
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15753550%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 January 2020
H Kua
series ordinal
4
1 reference
stated in
Europe PubMed Central
PMCID
1774468
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15753550%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 January 2020
R Ameratunga
series ordinal
5
1 reference
stated in
Europe PubMed Central
PMCID
1774468
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15753550%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 January 2020
language of work or name
English
0 references
publication date
1 April 2005
1 reference
stated in
Europe PubMed Central
PMCID
1774468
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15753550%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 January 2020
published in
Gut
1 reference
stated in
Europe PubMed Central
PMCID
1774468
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15753550%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 January 2020
volume
54
1 reference
stated in
Europe PubMed Central
PMCID
1774468
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15753550%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 January 2020
issue
4
1 reference
stated in
Europe PubMed Central
PMCID
1774468
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15753550%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 January 2020
page(s)
567-568
1 reference
stated in
Europe PubMed Central
PMCID
1774468
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15753550%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 January 2020
cites work
The ferroportin disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1774468
retrieved
28 May 2018
A valine deletion of ferroportin 1: a common mutation in hemochromastosis type 4
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1774468
retrieved
28 May 2018
Autosomal dominant reticuloendothelial iron overload associated with a 3-base pair deletion in the ferroportin 1 gene (SLC11A3)
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1774468
retrieved
28 May 2018
Novel mutation in ferroportin1 is associated with autosomal dominant hemochromatosis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1774468
retrieved
28 May 2018
A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1774468
retrieved
28 May 2018
Absence of hemochromatosis associated Cys282Tyr HFE gene mutation and low frequency of hemochromatosis phenotype in nonalcoholic chronic liver disease patients in India.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1774468
retrieved
16 August 2018
Genetic hyperferritinaemia and reticuloendothelial iron overload associated with a three base pair deletion in the coding region of the ferroportin gene (SLC11A3).
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1774468
retrieved
16 August 2018
Distribution of C282Y and H63D mutations in the HFE gene in healthy Asian Indians and patients with thalassaemia major
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/15753550
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Non-HFE hemochromatosis
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/15753550
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1136/GUT.2004.060988
1 reference
stated in
Europe PubMed Central
PMCID
1774468
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15753550%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 January 2020
PMCID
1774468
1 reference
stated in
Europe PubMed Central
PMCID
1774468
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15753550%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 January 2020
PubMed ID
15753550
1 reference
stated in
Europe PubMed Central
PMCID
1774468
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15753550%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 January 2020
15753551
reason for deprecated rank
incorrect identifier value
0 references
15753552
reason for deprecated rank
incorrect identifier value
0 references
ResearchGate publication ID
7979869
0 references
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