Familial frontotemporal dementia with parkinsonism associated with the progranulin c.C1021T (p.Q341X) mutation
- PMID: 20570546
- DOI: 10.1016/j.parkreldis.2010.05.001
Familial frontotemporal dementia with parkinsonism associated with the progranulin c.C1021T (p.Q341X) mutation
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