(Q35595902)

9 August 2017

0 references

A novel mutation in ferroportin1 is associated with haemochromatosis in a Solomon Islands patient (English)

1 reference

9 August 2017

1 reference

K E Arden

1

1 reference

9 August 2017

D F Wallace

2

1 reference

9 August 2017

J L Dixon

3

1 reference

9 August 2017

L Summerville

4

1 reference

9 August 2017

J W Searle

5

1 reference

9 August 2017

G J Anderson

6

1 reference

9 August 2017

G A Ramm

7

1 reference

9 August 2017

L W Powell

8

1 reference

9 August 2017

V N Subramaniam

9

1 reference

9 August 2017

language of work or name

English

0 references

publication date

1 August 2003

1 reference

9 August 2017

1 reference

9 August 2017

52

1 reference

9 August 2017

8

1 reference

9 August 2017

1215-1217

1 reference

Mutant antimicrobial peptide hepcidin is associated with severe juvenile hemochromatosis

9 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1773758

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1773758

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1773758

Novel mutation in ferroportin1 is associated with autosomal dominant hemochromatosis

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1773758

Autosomal-dominant hemochromatosis is associated with a mutation in the ferroportin (SLC11A3) gene

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1773758

A novel duodenal iron-regulated transporter, IREG1, implicated in the basolateral transfer of iron to the circulation

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1773758

The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1773758

Positional cloning of zebrafish ferroportin1 identifies a conserved vertebrate iron exporter

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1773758

Juvenile hemochromatosis locus maps to chromosome 1q.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1773758

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1773758

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1773758

A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1773758

A novel mammalian iron-regulated protein involved in intracellular iron metabolism

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1773758

Familial iron overload with possible autosomal dominant inheritance

26 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/12865285

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/GUT.52.8.1215

1 reference

9 August 2017

1 reference

9 August 2017

1 reference