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Rare Variants in PLXNA4 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 familial PD followed by frequency assess...
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| Asıl Yazarlar: | , , , , , , , , , , , , , , , , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Public Library of Science
2013
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3823607/ https://ncbi.nlm.nih.gov/pubmed/24244438 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0079145 |
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