טוען...
Screening for VPS35 mutations in Parkinson's disease
Recently 2 groups have independently identified a mutation in the gene ‘vacuolar protein sorting 35 homolog’ (VPS35 c.1858G>A; p.Asp620Asn) as a possible cause of autosomal dominant Parkinson's disease (PD). In order to assess the frequency of the reported mutation and to search for other po...
שמור ב:
| Main Authors: | , , , , , , , , , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Elsevier
2012
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3629567/ https://ncbi.nlm.nih.gov/pubmed/22154191 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neurobiolaging.2011.10.032 |
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