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Whole-genome sequencing suggests mechanisms for 22q11.2 deletion-associated Parkinson’s disease
OBJECTIVES: To investigate disease risk mechanisms of early-onset Parkinson’s disease (PD) associated with the recurrent 22q11.2 deletion, a genetic risk factor for early-onset PD. METHODS: In a proof-of-principle study, we used whole-genome sequencing (WGS) to investigate sequence variants in nine...
שמור ב:
| הוצא לאור ב: | PLoS One |
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| Main Authors: | , , , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Public Library of Science
2017
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5400231/ https://ncbi.nlm.nih.gov/pubmed/28430790 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0173944 |
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