APP, PSEN1, and PSEN2 mutations in early-onset Alzheimer disease: A genetic screening study of familial and sporadic cases-Reference-Cited by-同舟云学术

APP, PSEN1, and PSEN2 mutations in early-onset Alzheimer disease: A genetic screening study of familial and sporadic cases

Published:2017-03-28 Issue:3 Volume:14 Page:e1002270
ISSN:1549-1676
Container-title:PLOS Medicine
language:en
Short-container-title:PLoS Med

Author:

Lanoiselée Hélène-Marie,Nicolas Gaël,Wallon David,Rovelet-Lecrux Anne,Lacour Morgane,Rousseau Stéphane,Richard Anne-Claire,Pasquier Florence,Rollin-Sillaire Adeline,Martinaud Olivier,Quillard-Muraine Muriel,de la Sayette Vincent,Boutoleau-Bretonniere Claire,Etcharry-Bouyx Frédérique,Chauviré Valérie,Sarazin Marie,le Ber Isabelle,Epelbaum Stéphane,Jonveaux Thérèse,Rouaud Olivier,Ceccaldi Mathieu,Félician Olivier,Godefroy Olivier,Formaglio Maite,Croisile Bernard,Auriacombe Sophie,Chamard Ludivine,Vincent Jean-Louis,Sauvée Mathilde,Marelli-Tosi Cecilia,Gabelle Audrey,Ozsancak Canan,Pariente Jérémie,Paquet Claire,Hannequin Didier,Campion Dominique,

Funder

Clinical Research Hospital Program from the French Ministry of Health

French Ministry of Health

European Union

Publisher

Public Library of Science (PLoS)

Subject

General Medicine

Reference44 articles.

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2. Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease;R Sherrington;Nature,1995

3. A familial Alzheimer's disease locus on chromosome 1;E Levy-Lahad;Science,1995