A genome-wide study reveals rare CNVs exclusive to extreme phenotypes of Alzheimer disease.
Rovelet-Lecrux A; Legallic S; Wallon D; Flaman JM; Martinaud O; Bombois S; Rollin-Sillaire A; Michon A; Le Ber I; Pariente J; Puel M; Paquet C; Croisile B; Thomas-Antérion C; Vercelletto M; Lévy R; Frébourg T; Hannequin D; Campion D; European Journal Of Human Genetics: EJHG, 2012, vol. 20, issue 6, p 613, ISSN 14765438. ISBN 14765438.

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