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Significance of the parkin and PINK1 gene in Jordanian families with incidences of young-onset and juvenile parkinsonism
BACKGROUND: Parkinson's disease is a progressive neurodegenerative disorder, where most cases are sporadic with a late onset. In rare incidences familial forms of early-onset parkinsonism occur, and when recessively inherited, cases are often explained by mutations in either the parkin (PARK2)...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2008
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2635385/ https://ncbi.nlm.nih.gov/pubmed/19087301 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2377-8-47 |
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