A novel presenilin1 mutation (Q223R) associated with early onset Alzheimer’s disease, dysarthria and spastic paraparesis and decreased Abeta levels in CSF
Author:
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1468-1331.2009.02810.x/fullpdf
Reference10 articles.
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3. Inverse relation between in vivo amyloid imaging load and cerebrospinal fluid Abeta42 in humans;Fagan;Ann Neurol,2006
4. Clinical phenotypic heterogeneity of Alzheimer’s disease associated with mutations of the presenilin-1 gene;Larner;J Neurol,2006
5. Neuropsychological profiles of familial Alzheimer’s disease associated with mutations in the presenilin 1 and amyloid precursor protein genes;Warrington;J Neurol,2001
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3. Progressive cognitive impairment and familial spastic paraparesis due to PRESENILIN 1 mutation: anatomoclinical characterization;Journal of Neurology;2022-04-19
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