(Q46517228)

English

Inheritance of two HFE mutations in African Americans: cases with hemochromatosis phenotypes and estimates of hemochromatosis phenotype frequency.

scientific article published in July 2001

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scholarly article

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11478530%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

Inheritance of two HFE mutations in African Americans: cases with hemochromatosis phenotypes and estimates of hemochromatosis phenotype frequency (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11478530%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11478530%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

author name string

R T Acton

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11478530%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

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publication date

1 July 2001

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11478530%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

Genetics in Medicine

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11478530%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11478530%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11478530%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

294-300

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11478530%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

https://scigraph.springernature.com/pub.10.1097/00125817-200107000-00005

0 references

Primary iron overload in African Americans.

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200107000-00005

21 January 2018

Mutation analysis of the HFE gene associated with hereditary hemochromatosis in African Americans

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200107000-00005

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200107000-00005

21 January 2018

The effect of HFE genotypes on measurements of iron overload in patients attending a health appraisal clinic

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200107000-00005

21 January 2018

Practice guideline development task force of the College of American Pathologists. Hereditary hemochromatosis

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200107000-00005

21 January 2018

The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22.

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200107000-00005

21 January 2018

Hemochromatosis: association of severity of iron overload with genetic markers.

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200107000-00005

21 January 2018

Twenty-four hour variation of transferrin saturation in treated and untreated haemochromatosis homozygotes

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200107000-00005

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200107000-00005

21 January 2018

Dietary iron overload persists in rural sub-Saharan Africa

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200107000-00005

21 January 2018

Correlation between genotype and phenotype in hereditary hemochromatosis: analysis of 61 cases

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200107000-00005

21 January 2018

Global prevalence of putative haemochromatosis mutations

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200107000-00005

21 January 2018

Evidence from a Ghanaian population of known African descent to support the proposition that hemochromatosis is a Caucasian disorder

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200107000-00005

21 January 2018

Clinical and biochemical abnormalities in people heterozygous for hemochromatosis

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200107000-00005

21 January 2018

Absence of the hemochromatosis gene Cys282Tyr mutation in three ethnic groups from Algeria (Mzab), Ethiopia, and Senegal.

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200107000-00005

21 January 2018

Iron overload in African Americans

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200107000-00005

21 January 2018

Transferrin saturation phenotype and HFE genotype screening for hemochromatosis and primary iron overload: predictions from a model based on national, racial, and ethnic group composition in central Alabama

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200107000-00005

21 January 2018

Two novel missense mutations of the HFE gene (I105T and G93R) and identification of the S65C mutation in Alabama hemochromatosis probands

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200107000-00005

21 January 2018

A novel mutation of HFE explains the classical phenotype of genetic hemochromatosis in a C282Y heterozygote

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200107000-00005

21 January 2018

Two novel nonsense mutations of HFE gene in five unrelated italian patients with hemochromatosis

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200107000-00005

21 January 2018

Genetic and clinical description of hemochromatosis probands and heterozygotes: evidence that multiple genes linked to the major histocompatibility complex are responsible for hemochromatosis

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200107000-00005

21 January 2018

Transferrin receptor-2 (TFR2) mutation Y250X in Alabama Caucasian and African American subjects with and without primary iron overload

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200107000-00005

21 January 2018

HLA Phenotype and Haplotype Frequencies in the Cantabria (Middle North Spain) Population

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200107000-00005

21 January 2018

HLA-H mutations in the Ashkenazi Jewish population

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200107000-00005

21 January 2018

HLA as a marker of the hemochromatosis gene in Sweden

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200107000-00005

21 January 2018

Identifiers

10.1097/00125817-200107000-00005

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11478530%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11478530%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

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