(Q34989227)

5 August 2017

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title

HFE and non-HFE hemochromatosis (English)

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5 August 2017

Gregory J Anderson

1

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5 August 2017

Lawrie W Powell

series ordinal

2

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5 August 2017

publication date

1 October 2002

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International Journal of Hematology

5 August 2017

published in

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5 August 2017

volume

76

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5 August 2017

issue

3

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5 August 2017

page(s)

203-207

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A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis

5 August 2017

cites work

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12 December 2020

Iron and the genetics of cardiovascular disease

1 reference

12 December 2020

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

1 reference

12 December 2020

Familial iron overload with possible autosomal dominant inheritance

1 reference

12 December 2020

Noninvasive prediction of fibrosis in C282Y homozygous hemochromatosis

1 reference

12 December 2020

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

1 reference

12 December 2020

Hepatic iron concentration and total body iron stores in thalassemia major.

1 reference

12 December 2020

EASL International Consensus Conference on Haemochromatosis

1 reference

12 December 2020

Molecular medicine and hemochromatosis: at the crossroads

1 reference

12 December 2020

Iron uptake from plasma transferrin by the duodenum is impaired in the Hfe knockout mouse.

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Hereditary hemochromatosis in adults without pathogenic mutations in the hemochromatosis gene

1 reference

12 December 2020

Elevated serum type IV collagen: a sensitive indicator of the presence of cirrhosis in haemochromatosis

1 reference

12 December 2020

Ironing out disease: inherited disorders of iron homeostasis

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12 December 2020

Increased frequency of the haemochromatosis Cys282Tyr mutation in sporadic porphyria cutanea tarda

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12 December 2020

The C282Y mutation in the haemochromatosis gene (HFE) and hepatitis C virus infection are independent cofactors for porphyria cutanea tarda in Australian patients

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12 December 2020

High prevalence of the His63Asp HFE mutation in italian patients with porphyria cutanea tarda

1 reference

12 December 2020

Novel mutation in ferroportin1 is associated with autosomal dominant hemochromatosis

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12 December 2020

Genetics of hemochromatosis

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12 December 2020

Diagnosis and management of hemochromatosis.

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12 December 2020

Identifiers

DOI

10.1007/BF02982788

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Dimensions Publication ID

5 August 2017

1040036518

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Fatcat ID

release_4at3zn7sojan3fxblatg3aj2bq

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Fatcat

https://api.fatcat.wiki/v0/release/4at3zn7sojan3fxblatg3aj2bq

24 November 2022

mapped directly with Wikidata item

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