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English
Ferroportin disease due to the A77D mutation in Australia.
scientific article published in July 2005
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
1774624
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15951560%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 January 2020
title
Ferroportin disease due to the A77D mutation in Australia
(English)
1 reference
stated in
Europe PubMed Central
PMCID
1774624
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15951560%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 January 2020
main subject
Australia
0 references
author
Nathan V Subramaniam
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
1774624
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15951560%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 January 2020
Daniel F. Wallace
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMCID
1774624
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15951560%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 January 2020
author name string
J L Dixon
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMCID
1774624
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15951560%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 January 2020
L M Fletcher
series ordinal
4
1 reference
stated in
Europe PubMed Central
PMCID
1774624
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15951560%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 January 2020
D H Crawford
series ordinal
5
1 reference
stated in
Europe PubMed Central
PMCID
1774624
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15951560%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 January 2020
language of work or name
English
0 references
publication date
1 July 2005
1 reference
stated in
Europe PubMed Central
PMCID
1774624
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15951560%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 January 2020
published in
Gut
1 reference
stated in
Europe PubMed Central
PMCID
1774624
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15951560%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 January 2020
volume
54
1 reference
stated in
Europe PubMed Central
PMCID
1774624
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15951560%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 January 2020
issue
7
1 reference
stated in
Europe PubMed Central
PMCID
1774624
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15951560%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 January 2020
page(s)
1048-1049
1 reference
stated in
Europe PubMed Central
PMCID
1774624
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15951560%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 January 2020
cites work
Identification of ferroportin disease in the Indian subcontinent.
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=1774624
retrieved
26 May 2018
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=1774624
retrieved
26 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=1774624
retrieved
26 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=1774624
retrieved
26 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=1774624
retrieved
26 May 2018
Autosomal-dominant hemochromatosis is associated with a mutation in the ferroportin (SLC11A3) gene
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=1774624
retrieved
26 May 2018
A mutation in SLC11A3 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=1774624
retrieved
26 May 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=1774624
retrieved
16 August 2018
Identifiers
DOI
10.1136/GUT.2005.069021
1 reference
stated in
Europe PubMed Central
PMCID
1774624
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15951560%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 January 2020
PMCID
1774624
1 reference
stated in
Europe PubMed Central
PMCID
1774624
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15951560%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 January 2020
PubMed ID
15951560
1 reference
stated in
Europe PubMed Central
PMCID
1774624
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15951560%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 January 2020
ResearchGate publication ID
7790308
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