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Rare variants in LRRK1 and Parkinson's disease
Approximately 20 % of individuals with Parkinson's disease (PD) report a positive family history. Yet, a large portion of causal and disease-modifying variants is still unknown. We used exome sequencing in two affected individuals from a family with late-onset PD to identify 15 potentially caus...
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| Main Authors: | , , , , , , , , , , , , , , , , , , , , , |
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| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Springer Berlin Heidelberg
2013
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3968516/ https://ncbi.nlm.nih.gov/pubmed/24241507 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10048-013-0383-8 |
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