The 16189 variant of mitochondrial DNA occurs more frequently in C282Y homozygotes with haemochromatosis than those without iron loading

Background:Patients with hereditary haemochromatosis (HH) are usually homozygous for the C282Y mutation in the HFE gene. They have variable expression of iron overload and present with a variety of complications, including liver disease, diabetes, arthropathy, fatigue, and cardiomyopathy. The mitoch...

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Detalhes bibliográficos
Main Authors: Livesey, K, Wimhurst, V, Carter, K, Worwood, M, Cadet, E, Rochette, J, Roberts, A, Pointon, J, Merryweather-Clar..., A, Bassett, M, Jouanolle, A, Mosser, A, David, V, Poulton, J, Robson, K
Formato: Artigo
Idioma:Inglês
Publicado em: BMJ Group 2004
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Original Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1757237/
https://ncbi.nlm.nih.gov/pubmed/14729817
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2003.008805
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