(Q54359179)

English

Prevalence of the C282Y and H63D mutations in the HFE gene in patients with hereditary haemochromatosis and in control subjects from Northern Germany.

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scholarly article

1 reference

Europe PubMed Central

28 May 2018

http://europepmc.org/abstract/MED/9858243

Prevalence of the C282Y and H63D mutations in the HFE gene in patients with hereditary haemochromatosis and in control subjects from Northern Germany. (English)

1 reference

Europe PubMed Central

28 May 2018

http://europepmc.org/abstract/MED/9858243

0 references

5

1 reference

Europe PubMed Central

28 May 2018

http://europepmc.org/abstract/MED/9858243

author name string

Nielsen P

1

1 reference

Europe PubMed Central

28 May 2018

http://europepmc.org/abstract/MED/9858243

Carpinteiro S

2

1 reference

Europe PubMed Central

28 May 2018

http://europepmc.org/abstract/MED/9858243

Fischer R

3

1 reference

Europe PubMed Central

28 May 2018

http://europepmc.org/abstract/MED/9858243

Cabeda JM

4

1 reference

Europe PubMed Central

28 May 2018

http://europepmc.org/abstract/MED/9858243

Gabbe EE

6

1 reference

Europe PubMed Central

28 May 2018

http://europepmc.org/abstract/MED/9858243

language of work or name

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publication date

1 December 1998

1 reference

Europe PubMed Central

28 May 2018

http://europepmc.org/abstract/MED/9858243

British Journal of Haematology

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Europe PubMed Central

28 May 2018

http://europepmc.org/abstract/MED/9858243

103

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Europe PubMed Central

28 May 2018

http://europepmc.org/abstract/MED/9858243

3

1 reference

Europe PubMed Central

28 May 2018

http://europepmc.org/abstract/MED/9858243

842-845

1 reference

Europe PubMed Central

28 May 2018

http://europepmc.org/abstract/MED/9858243

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

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.1998.01037.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.1998.01037.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.1998.01037.X

21 January 2018

Haemochromatosis and HLA-H.

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.1998.01037.X

21 January 2018

A candidate gene for hemochromatosis: frequency of the C282Y and H63D mutations.

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.1998.01037.X

21 January 2018

Global prevalence of putative haemochromatosis mutations

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.1998.01037.X

21 January 2018

Identifiers

10.1046/J.1365-2141.1998.01037.X

1 reference

Europe PubMed Central

28 May 2018

http://europepmc.org/abstract/MED/9858243

1 reference

Europe PubMed Central

28 May 2018

http://europepmc.org/abstract/MED/9858243

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