PINK1 mutations and parkinsonism

BACKGROUND: PINK1 loss-of-function causes recessive, early-onset parkinsonism. In Tunisia there is a high rate of consanguineous marriage but PINK1 carrier frequency and disease prevalence have yet to be assessed. OBJECTIVES: The frequency of PINK1 mutations in familial parkinsonism, community-based...

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Detalhes bibliográficos
Main Authors: Ishihara-Paul, L, Hulihan, M M., Kachergus, J, Upmanyu, R, Warren, L, Amouri, R, Elango, R, Prinjha, R K., Soto, A, Kefi, M, Zouari, M, Sassi, S B., Yahmed, S B., El Euch-Fayeche, G, Matthews, P M., Middleton, L T., Gibson, R A., Hentati, F, Farrer, M J.
Formato: Artigo
Idioma:Inglês
Publicado em: American Academy of Neurology 2008
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Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2676945/
https://ncbi.nlm.nih.gov/pubmed/18685134
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/01.wnl.0000323812.40708.1f
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