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Prevalence of haemochromatosis gene mutations in Parkinson's disease

The aim of this study was to investigate a possible association between haemochromatosis (HFE) gene mutations and the prevalence of Parkinson's disease. The HFE gene encodes a protein that modulates iron absorption. Several studies have documented increased iron levels in the basal ganglia in p...

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Detalhes bibliográficos
Main Authors: Aamodt, Anne Hege, Stovner, Lars Jacob, Thorstensen, Ketil, Lydersen, Stian, White, Linda R, Aasly, Jan O
Formato: Artigo
Idioma:Inglês
Publicado em: BMJ Group 2007
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2117639/
https://ncbi.nlm.nih.gov/pubmed/17056630
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jnnp.2006.101352
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