(Q43104941)

14 November 2017

The significance of the 187G (H63D) mutation in hemochromatosis (English)

1 reference

14 November 2017

E Beutler

1

1 reference

PMC publication ID

1715965

14 November 2017

language of work or name

English

0 references

publication date

1 September 1997

1 reference

American Journal of Human Genetics

14 November 2017

1 reference

14 November 2017

61

1 reference

14 November 2017

3

1 reference

14 November 2017

762-764

1 reference

HLA-H and associated proteins in patients with hemochromatosis

14 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715965

Mutation analysis of the HLA-H gene in Italian hemochromatosis patients

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715965

Mutation analysis in hereditary hemochromatosis

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715965

Defective iron homeostasis in beta 2-microglobulin knockout mice recapitulates hereditary hemochromatosis in man.

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715965

Haemochromatosis and HLA-H.

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715965

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

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715965

beta2 knockout mice develop parenchymal iron overload: A putative role for class I genes of the major histocompatibility complex in iron metabolism

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715965

Haplotype analysis in Australian hemochromatosis patients: evidence for a predominant ancestral haplotype exclusively associated with hemochromatosis

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715965

Genetic irony beyond haemochromatosis: clinical effects of HLA-H mutations

25 May 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9297%2807%2964339-0

HLA-H mutations in the Ashkenazi Jewish population

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9297%2807%2964339-0

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9297%2807%2964339-0

Mutations in the MHC class I-like candidate gene for hemochromatosis in French patients

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9297%2807%2964339-0

Haemochromatosis and HLA-H

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9297%2807%2964339-0

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9297%2807%2964339-0

10.1016/S0002-9297(07)64339-0

7 January 2021

Identifiers

DOI

1 reference

14 November 2017

1 reference

PMC publication ID

1715965

14 November 2017

PubMed publication ID

9326341

1 reference

PMC publication ID

1715965