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HFE genotypes, haemochromatosis diagnosis and clinical outcomes at age 80 years: a prospective cohor...

HFE genotypes, haemochromatosis diagnosis and clinical outcomes at age 80 years: a prospective cohor...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_22d52cd1e74b4e34a09f5de25b2cdaa1

HFE genotypes, haemochromatosis diagnosis and clinical outcomes at age 80 years: a prospective cohort study in the UK Biobank

About this item

Full title

HFE genotypes, haemochromatosis diagnosis and clinical outcomes at age 80 years: a prospective cohort study in the UK Biobank

Publisher

England: British Medical Journal Publishing Group

Journal title

BMJ open, 2024-03, Vol.14 (3), p.e081926

Language

English

Formats

Publication information

Publisher

England: British Medical Journal Publishing Group

More information

Scope and Contents

Contents

ObjectivesHFE haemochromatosis genetic variants have an uncertain clinical penetrance, especially to older ages and in undiagnosed groups. We estimated p.C282Y and p.H63D variant cumulative incidence of multiple clinical outcomes in a large community cohort.DesignProspective cohort study.Setting22 assessment centres across England, Scotland, and Wa...

Alternative Titles

Full title

HFE genotypes, haemochromatosis diagnosis and clinical outcomes at age 80 years: a prospective cohort study in the UK Biobank

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_22d52cd1e74b4e34a09f5de25b2cdaa1

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_22d52cd1e74b4e34a09f5de25b2cdaa1

Other Identifiers

ISSN

2044-6055

E-ISSN

2044-6055

DOI

10.1136/bmjopen-2023-081926

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