(Q28237178)

2 July 2017

title

Global prevalence of putative haemochromatosis mutations (English)

1 reference

2 July 2017

author name string

A T Merryweather-Clarke

1

1 reference

2 July 2017

J J Pointon

2

1 reference

2 July 2017

J D Shearman

3

1 reference

2 July 2017

K J Robson

4

1 reference

2 July 2017

language of work or name

English

0 references

publication date

1 April 1997

1 reference

Journal of Medical Genetics

2 July 2017

published in

1 reference

2 July 2017

volume

34

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2 July 2017

issue

4

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2 July 2017

page(s)

275-278

1 reference

A genome screen in multiple sclerosis reveals susceptibility loci on chromosome 6p21 and 17q22

2 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050911

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

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050911

Molecular basis of cystathionine beta-synthase deficiency in pyridoxine responsive and nonresponsive homocystinuria

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050911

Mutation in the iron responsive element of the L ferritin mRNA in a family with dominant hyperferritinaemia and cataract

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050911

Molecular basis for the recently described hereditary hyperferritinemia-cataract syndrome: a mutation in the iron-responsive element of ferritin L-subunit gene (the "Verona mutation")

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050911

Iron overload in Africa. Interaction between a gene and dietary iron content

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050911

A genome-wide search for quantitative trait loci underlying asthma

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050911

The origin of the major cystic fibrosis mutation (delta F508) in European populations.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050911

Increased risk of skin cancer: another Celtic myth? A review of Celtic ancestry and other risk factors for malignant melanoma and nonmelanoma skin cancer.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050911

Human genomic diversity in Europe: a summary of recent research and prospects for the future

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050911

A study of 609 HLA haplotypes marking for the hemochromatosis gene: (1) mapping of the gene near the HLA-A locus and characters required to define a heterozygous population and (2) hypothesis concerning the underlying cause of hemochromatosis-HLA as

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050911

Mutation analysis in hereditary hemochromatosis

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050911

Haemochromatosis and HLA-H.

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050911

DNA restriction fragments associated with alpha 1-antitrypsin indicate a single origin for deficiency allele PI Z.

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050911

Serum Ferritin as a Possible Marker of the Hemochromatosis Allele

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050911

Primary iron overload in African Americans

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050911

Hereditary iron overload and African Americans

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050911

Haemochromatosis and HLA-H

27 November 2018

1 reference

12 December 2020

IDIOPATHIC AND BANTU HEMOCHROMATOSIS. COMPARATIVE HISTOLOGICAL STUDY

1 reference

12 December 2020

HEMOCHROMATOSIS AND CIRRHOSIS IN DIFFERENT GEOGRAPHIC AREAS

1 reference

12 December 2020

A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex. The Multiple Sclerosis Genetics Group

1 reference

12 December 2020

Letter: Idiopathic hemochromatosis associated with HL-A 3 tissular antigen

1 reference

12 December 2020

Prevalence of iron overload in central Sweden

1 reference

12 December 2020

Prevalence of Hemochromatosis among 11,065 Presumably Healthy Blood Donors

1 reference

12 December 2020

Prevalence of hemochromatosis in Finland

1 reference

12 December 2020

Prevalence of haemochromatosis amongst asymptomatic Australians

1 reference

12 December 2020

Familial iron overload with possible autosomal dominant inheritance

1 reference

12 December 2020

'Celtic' phenylketonuria chromosomes found? Evidence in two regions of Quebec Province

1 reference

12 December 2020

Screening blood donors for hereditary hemochromatosis: decision analysis model based on a 30-year database

1 reference

12 December 2020

Non-HLA-linked hemochromatosis in a Chinese woman

1 reference

12 December 2020

Iron overload in African Americans

1 reference

12 December 2020

Long-term survival in patients with hereditary hemochromatosis

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.34.4.275

1 reference

OpenCitations bibliographic resource ID

2 July 2017

4418369

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

4418369

1 reference