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Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration. [electronic resource] by
Producer: 20150608 In: Acta neuropathologica vol. 128
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TBK1 Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis. [electronic resource] by
Producer: 20171222 In: Human mutation vol. 38
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A pan-European study of the C9orf72 repeat associated with FTLD: geographic prevalence, genomic instability, and intermediate repeats. [electronic resource] by
Producer: 20130726 In: Human mutation vol. 34
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Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study. [electronic resource] by
Producer: 20200715 In: The Lancet. Neurology vol. 19
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Association of Cerebral Amyloid-β Aggregation With Cognitive Functioning in Persons Without Dementia. [electronic resource] by
Producer: 20190912 In: JAMA psychiatry vol. 75
Availability: No items available.