Early-Onset Familial Alzheimer Disease Variant PSEN2 N141I Heterozygosity is Associated with Altered Microglia Phenotype.

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Bibliographic Details
Title: Early-Onset Familial Alzheimer Disease Variant PSEN2 N141I Heterozygosity is Associated with Altered Microglia Phenotype.
Authors: Fung S; Department of Neurology, University of Washington, Seattle, WA, USA., Smith CL; Department of Neurology, University of Washington, Seattle, WA, USA., Prater KE; Department of Neurology, University of Washington, Seattle, WA, USA., Case A; Department of Neurology, University of Washington, Seattle, WA, USA., Green K; Department of Neurology, University of Washington, Seattle, WA, USA., Osnis L; Department of Neurology, University of Washington, Seattle, WA, USA., Winston C; Department of Neurology, University of Washington, Seattle, WA, USA., Kinoshita Y; Department of Neurosurgery, University of Washington, Seattle, WA, USA., Sopher B; Department of Neurology, University of Washington, Seattle, WA, USA., Morrison RS; Department of Neurosurgery, University of Washington, Seattle, WA, USA., Garden GA; Department of Neurology, University of North Carolina, Chapel Hill, NC, USA., Jayadev S; Department of Neurology, University of Washington, Seattle, WA, USA.
Source: Journal of Alzheimer's disease : JAD [J Alzheimers Dis] 2020; Vol. 77 (2), pp. 675-688.
Publication Type: Journal Article; Research Support, N.I.H., Extramural
Journal Info: Publisher: SAGE Publications Country of Publication: United States NLM ID: 9814863 Publication Model: Print Cited Medium: Internet ISSN: 1875-8908 (Electronic) Linking ISSN: 13872877 NLM ISO Abbreviation: J Alzheimers Dis Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1875-8908
DOI:10.3233/JAD-200492