The evaluation of hyperferritinemia: an updated strategy based on advances in detecting genetic abnormalities. (Q36103131)

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11 January 2020

review article

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title

The evaluation of hyperferritinemia: an updated strategy based on advances in detecting genetic abnormalities (English)

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11 January 2020

2

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11 January 2020

author name string

Patricia Aguilar-Martinez

series ordinal

1

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11 January 2020

Pierre Brissot

series ordinal

3

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11 January 2020

language of work or name

English

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publication date

1 May 2005

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The American Journal of Gastroenterology

11 January 2020

published in

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11 January 2020

volume

100

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11 January 2020

page(s)

1185-1194

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11 January 2020

issue

5

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

11 January 2020

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Digenic inheritance of mutations in HAMP and HFE results in different types of haemochromatosis

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Transferrin receptor-2 gene and non-C282Y homozygous patients with hemochromatosis.

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Transferrin receptor 2 (TfR2) and HFE mutational analysis in non-C282Y iron overload: identification of a novel TfR2 mutation

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Mutations in HFE2 cause iron overload in chromosome 1q-linked juvenile hemochromatosis

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Scanning mutations of the 5'UTR regulatory sequence of l-ferritin by denaturing high-performance liquid chromatography: identification of new mutations

21 January 2018

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10.1111/J.1572-0241.2005.40998.X

21 January 2018

Identifiers

DOI

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11 January 2020

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