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Rare variants in β-Amyloid precursor protein (APP) and Parkinson's disease
Many individuals with Parkinson's disease (PD) develop cognitive deficits, and a phenotypic and molecular overlap between neurodegenerative diseases exists. We investigated the contribution of rare variants in seven genes of known relevance to dementias (β-amyloid precursor protein (APP), PSEN1...
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| Publicado no: | Eur J Hum Genet |
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| Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Publishing Group
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4592093/ https://ncbi.nlm.nih.gov/pubmed/25604855 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2014.300 |
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