(Q44827980)

6 December 2017

title

High prevalence of non-HFE gene-associated haemochromatosis in patients from southern Italy (English)

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6 December 2017

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5

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6 December 2017

Francesco De Marco

1

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6 December 2017

Rosario Liguori

2

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6 December 2017

Maria Grazia Giardina

3

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6 December 2017

Maria D'Armiento

4

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6 December 2017

Antonio Lucariello

6

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6 December 2017

Roberto Morante

7

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6 December 2017

Lucia Cimino

8

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6 December 2017

Alfonso Galeota-Lanza

9

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6 December 2017

Giovanni Tarantino

10

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6 December 2017

Antonio Ascione

11

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6 December 2017

Gabriele Budillon

12

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6 December 2017

Raffaela Vecchione

13

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6 December 2017

Rosanna Martinelli

14

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6 December 2017

Margherita Matarazzo

15

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6 December 2017

Vincenzo De Simone

16

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6 December 2017

publication date

1 January 2004

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Clinical Chemistry and Laboratory Medicine

6 December 2017

published in

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6 December 2017

volume

42

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6 December 2017

issue

1

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6 December 2017

page(s)

17-24

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

6 December 2017

cites work

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https://api.crossref.org/works/10.1515%2FCCLM.2004.005

Mechanism of increased iron absorption in murine model of hereditary hemochromatosis: increased duodenal expression of the iron transporter DMT1

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2004.005

Association of HFE protein with transferrin receptor in crypt enterocytes of human duodenum

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2004.005

Mutation analysis in hereditary hemochromatosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2004.005

Hepatic iron overload in patients with chronic viral hepatitis: role of HFE gene mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2004.005

A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2004.005

The hemochromatosis founder mutation in HLA-H disrupts beta2-microglobulin interaction and cell surface expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2004.005

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2004.005

Recent advances in disorders of iron metabolism: mutations, mechanisms and modifiers

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2004.005

Novel mutation in ferroportin1 is associated with autosomal dominant hemochromatosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2004.005

Prevalence of hereditary hemochromatosis in a Massachusetts corporation: is Celtic origin a risk factor?

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2004.005

Juvenile hemochromatosis locus maps to chromosome 1q.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2004.005

Haemochromatosis and HLA-H.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2004.005

Molecular aspects of iron absorption and HFE expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2004.005

Prevalence, risk factors, and genotype distribution of hepatitis C virus infection in the general population: a community-based survey in southern Italy

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2004.005

Crystal structure of the hemochromatosis protein HFE and characterization of its interaction with transferrin receptor

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2004.005

Genotypic/phenotypic correlations in genetic hemochromatosis: evolution of diagnostic criteria.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2004.005

Histological assessment of liver siderosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2004.005

Hemochromatosis after the gene discovery: revisiting the diagnostic strategy

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2004.005

HFE gene knockout produces mouse model of hereditary hemochromatosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2004.005

Variable phenotypic presentation of iron overload in H63D homozygotes: are genetic modifiers the cause?

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2004.005

The hemochromatosis gene product complexes with the transferrin receptor and lowers its affinity for ligand binding

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2004.005

21 January 2018

Identifiers

DOI

10.1515/CCLM.2004.005

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6 December 2017

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