Common conditions associated with hereditary haemochromatosis genetic variants: cohort study in UK Biobank

OBJECTIVE: To compare prevalent and incident morbidity and mortality between those with the HFE p.C282Y genetic variant (responsible for most hereditary haemochromatosis type 1) and those with no p.C282Y mutations, in a large UK community sample of European descent. DESIGN: Cohort study. SETTING: 22...

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Detalles Bibliográficos
Autores principales: Pilling, Luke C, Tamosauskaite, Jone, Jones, Garan, Wood, Andrew R, Jones, Lindsay, Kuo, Chai-Ling, Kuchel, George A, Ferrucci, Luigi, Melzer, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group Ltd. 2019
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6334179/
https://www.ncbi.nlm.nih.gov/pubmed/30651232
http://dx.doi.org/10.1136/bmj.k5222

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6334179/
https://www.ncbi.nlm.nih.gov/pubmed/30651232
http://dx.doi.org/10.1136/bmj.k5222

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