(Q44198084)

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

scientific article published in November 2002

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14 December 2019

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

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14 December 2019

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14 December 2019

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14 December 2019

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14 December 2019

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Mario Cazzola

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14 December 2019

Laura Cremonesi

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14 December 2019

Maria Papaioannou

3

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14 December 2019

Nadia Soriani

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14 December 2019

Anna Kioumi

5

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14 December 2019

Anastasia Charalambidou

6

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14 December 2019

Katerina Romtsou

8

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14 December 2019

Maurizio Ferrari

10

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14 December 2019

John Christakis

12

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14 December 2019

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1 November 2002

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14 December 2019

British Journal of Haematology

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14 December 2019

119

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14 December 2019

2

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14 December 2019

539-546

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14 December 2019

A mammalian iron ATPase induced by iron.

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.2002.03946.X

21 January 2018

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/10.1046%2FJ.1365-2141.2002.03946.X

21 January 2018

Positional cloning of zebrafish ferroportin1 identifies a conserved vertebrate iron exporter

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.2002.03946.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.2002.03946.X

21 January 2018

A study of genes that may modulate the expression of hereditary hemochromatosis: transferrin receptor-1, ferroportin, ceruloplasmin, ferritin light and heavy chains, iron regulatory proteins (IRP)-1 and -2, and hepcidin

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.2002.03946.X

21 January 2018

A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.2002.03946.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.2002.03946.X

21 January 2018

Regulation of ferritin genes and protein

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.2002.03946.X

21 January 2018

Novel mutation in ferroportin1 is associated with autosomal dominant hemochromatosis

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.2002.03946.X

21 January 2018

Denaturing high-performance liquid chromatography: A review

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.2002.03946.X

21 January 2018

A novel deletion of the l-ferritin iron-responsive element responsible for severe hereditary hyperferritinaemia-cataract syndrome

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.2002.03946.X

21 January 2018

Short direct repeats at the breakpoints of a novel large deletion in the CFTR gene suggest a likely slipped mispairing mechanism

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.2002.03946.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.2002.03946.X

21 January 2018

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