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Integrative multiomics reveals common endotypes across PSEN1, PSEN2, and APP mutations in familial Alzheimer's disease.

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Bibliographic Details
Title:	Integrative multiomics reveals common endotypes across PSEN1, PSEN2, and APP mutations in familial Alzheimer's disease.
Authors:	Valdes, Phoebe^1,2 (AUTHOR), Caldwell, Andrew B.¹ (AUTHOR), Liu, Qing^3,4 (AUTHOR), Fitzgerald, Michael Q.^1,2 (AUTHOR), Ramachandran, Srinivasan¹ (AUTHOR), Karch, Celeste M.⁵ (AUTHOR), Adams, Sarah (AUTHOR), Allegri, Ricardo (AUTHOR), Araki, Aki (AUTHOR), Barthelemy, Nicolas (AUTHOR), Bateman, Randall (AUTHOR), Bechara, Jacob (AUTHOR), Benzinger, Tammie (AUTHOR), Berman, Sarah (AUTHOR), Bodge, Courtney (AUTHOR), Brandon, Susan (AUTHOR), Brooks, William Bill (AUTHOR), Brosch, Jared (AUTHOR), Buck, Jill (AUTHOR), Buckles, Virginia (AUTHOR)
Source:	Alzheimer's Research & Therapy. 1/3/2025, Vol. 17 Issue 1, p1-20. 20p.
Database:	Academic Search Ultimate
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Description
ISSN:	17589193
DOI:	10.1186/s13195-024-01659-6