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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)...
| Autores principales: | , , , , , , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2008
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2635385/ https://www.ncbi.nlm.nih.gov/pubmed/19087301 http://dx.doi.org/10.1186/1471-2377-8-47 |