(Q44520890)

3 December 2017

title

Novel mutation in ferroportin 1 gene is associated with autosomal dominant iron overload (English)

1 reference

3 December 2017

Anne-Marie Jouanolle

1

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3 December 2017

Véronique Douabin-Gicquel

2

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3 December 2017

Chantal Halimi

3

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3 December 2017

Olivier Loréal

4

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3 December 2017

Patricia Fergelot

5

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3 December 2017

Thierry Delacour

6

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3 December 2017

Anne-Sophie de Lajarte-Thirouard

7

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3 December 2017

Bruno Turlin

8

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3 December 2017

Jean-Yves Le Gall

9

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3 December 2017

Estelle Cadet

10

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3 December 2017

Jacques Rochette

11

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3 December 2017

Véronique David

12

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3 December 2017

Pierre Brissot

13

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3 December 2017

publication date

1 August 2003

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3 December 2017

published in

Journal of Hepatology

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3 December 2017

volume

39

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3 December 2017

issue

2

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3 December 2017

page(s)

286-289

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A genotypic study of 217 unrelated probands diagnosed as "genetic hemochromatosis" on "classical" phenotypic criteria

3 December 2017

cites work

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7 January 2021

Juvenile hemochromatosis locus maps to chromosome 1q.

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7 January 2021

New mutations inactivating transferrin receptor 2 in hemochromatosis type 3.

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2803%2900148-X

7 January 2021

A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis

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https://api.crossref.org/works/10.1016%2FS0168-8278%2803%2900148-X

7 January 2021

Positional cloning of zebrafish ferroportin1 identifies a conserved vertebrate iron exporter

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7 January 2021

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

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7 January 2021

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

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7 January 2021

A mutation, in the iron-responsive element of H ferritin mRNA, causing autosomal dominant iron overload

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https://api.crossref.org/works/10.1016%2FS0168-8278%2803%2900148-X

7 January 2021

A mutation in the ceruloplasmin gene is associated with systemic hemosiderosis in humans

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7 January 2021

Aceruloplasminemia: new clinical, pathophysiological and therapeutic insights

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7 January 2021

A new syndrome of liver iron overload with normal transferrin saturation

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7 January 2021

Insulin resistance-associated hepatic iron overload.

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7 January 2021

Measurement of liver-iron concentration in needle-biopsy specimens

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7 January 2021

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

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7 January 2021

Multicentric origin of hemochromatosis gene (HFE) mutations

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7 January 2021

Molecular cloning of transferrin receptor 2. A new member of the transferrin receptor-like family

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7 January 2021

Glycine and beta-branched residues support and modulate peptide helicity in membrane environments

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https://api.crossref.org/works/10.1016%2FS0168-8278%2803%2900148-X

7 January 2021

Novel mutation in ferroportin1 is associated with autosomal dominant hemochromatosis

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2803%2900148-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2803%2900148-X

7 January 2021

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

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7 January 2021

Helix packing in polytopic membrane proteins: role of glycine in transmembrane helix association

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7 January 2021

Ferroportin mutation in autosomal dominant hemochromatosis: loss of function, gain in understanding

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2803%2900148-X

7 January 2021

10.1016/S0168-8278(03)00148-X

Identifiers

DOI

1 reference

release_ycnfckb5ancazovjytcvvetv7q

3 December 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/ycnfckb5ancazovjytcvvetv7q

24 November 2022

mapped directly with Wikidata item

1 reference