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Implications and frequency of APP, PSEN1, PSEN2, GRN and MAPT mutation in a well-characterized series of late-onset Alzheimer families

✍ Scribed by Carlos Cruchaga; Sumi Chakraverty; Gabe Haller; Mayo Kevin; Francesco L. Vallania; Mitra D. Robi; Tom D. Bird; Ramón Diaz-Arrestia; Bradley Boeve; Boeve Bradley; Neill R. Graff-Radford; Richard Mayeux; Alison Goate


Book ID
118466391
Publisher
Elsevier Science
Year
2010
Tongue
English
Weight
47 KB
Volume
6
Category
Article
ISSN
1552-5260

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