ABCA7 rare variants and Alzheimer disease risk

OBJECTIVE: To study the association between ABCA7 rare coding variants and Alzheimer disease (AD) in a case-control setting. METHODS: We conducted a whole exome analysis among 484 French patients with early-onset AD and 590 ethnically matched controls. RESULTS: After collapsing rare variants (minor...

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Bibliografski detalji
Izdano u:Neurology
Glavni autori: Le Guennec, Kilan, Nicolas, Gaël, Quenez, Olivier, Charbonnier, Camille, Wallon, David, Bellenguez, Céline, Grenier-Boley, Benjamin, Rousseau, Stéphane, Richard, Anne-Claire, Rovelet-Lecrux, Anne, Bacq, Delphine, Garnier, Jean-Guillaume, Olaso, Robert, Boland, Anne, Meyer, Vincent, Deleuze, Jean-François, Amouyel, Philippe, Munter, Hans Markus, Bourque, Guillaume, Lathrop, Mark, Frebourg, Thierry, Redon, Richard, Letenneur, Luc, Dartigues, Jean-François, Pasquier, Florence, Rollin-Sillaire, Adeline, Génin, Emmanuelle, Lambert, Jean-Charles, Hannequin, Didier, Campion, Dominique
Format: Artigo
Jezik:Inglês
Izdano: Lippincott Williams & Wilkins 2016
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Article
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4898320/
https://ncbi.nlm.nih.gov/pubmed/27037229
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/WNL.0000000000002627
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