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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Vydáno v:BMJ
Hlavní autoři: Pilling, Luke C, Tamosauskaite, Jone, Jones, Garan, Wood, Andrew R, Jones, Lindsay, Kuo, Chai-Ling, Kuchel, George A, Ferrucci, Luigi, Melzer, David
Médium: Artigo
Jazyk:Inglês
Vydáno: BMJ Publishing Group Ltd. 2019
Témata:
Research
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6334179/
https://ncbi.nlm.nih.gov/pubmed/30651232
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bmj.k5222
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