Parkin Disease: A Clinicopathologic Entity?

IMPORTANCE: Mutations in the gene encoding parkin (PARK2) are the most common cause of autosomal recessive juvenile-onset and young-onset parkinsonism. The few available detailed neuropathologic reports suggest that homozygous and compound heterozygous parkin mutations are characterized by severe su...

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Detalhes bibliográficos
Main Authors: Doherty, Karen M., Silveira-Moriyama, Laura, Parkkinen, Laura, Healy, Daniel G., Farrell, Michael, Mencacci, Niccolo E., Ahmed, Zeshan, Brett, Francesca M., Hardy, John, Quinn, Niall, Counihan, Timothy J., Lynch, Timothy, Fox, Zoe V., Revesz, Tamas, Lees, Andrew J., Holton, Janice L.
Formato: Artigo
Idioma:Inglês
Publicado em: 2013
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4202385/
https://ncbi.nlm.nih.gov/pubmed/23459986
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1001/jamaneurol.2013.172
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