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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Aamodt, Anne Hege, Stovner, Lars Jacob, Thorstensen, Ketil, Lydersen, Stian, White, Linda R, Aasly, Jan O
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: BMJ Group 2007
Gaiak:
Short Report
Sarrera elektronikoa: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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