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Homozygous deletion mutation of the parkin gene in patients with atypical parkinsonism
Autosomal recessive juvenile parkinsonism (AR-JP) is characterised by homogenous clinical features and selective degeneration of nigral neurons. Recent progress in molecular genetic analyses of AR-JP has led to the identification of a novel ubiquitin-like protein, parkin, whose precise function stil...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMJ Group
2001
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1737499/ https://ncbi.nlm.nih.gov/pubmed/11459900 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jnnp.71.2.231 |
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