Common conditions associated with hereditary haemochromatosis genetic variants: cohort study in UK Biobank
OPEN BMJ (Clinical research ed.) | 18 Jan 2019
LC Pilling, J Tamosauskaite, G Jones, AR Wood, L Jones, CL Kuo, GA Kuchel, L Ferrucci and D Melzer
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.
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