المؤلفون: Rovelet-Lecrux A; Inserm U614, Faculté de Médecine, Rouen, France., 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

مؤلفون مشاركون: Investigators of the GMAJ project

المصدر: European journal of human genetics : EJHG [Eur J Hum Genet] 2012 Jun; Vol. 20 (6), pp. 613-7. Date of Electronic Publication: 2011 Dec 14.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5438 (Electronic) Linking ISSN: 10184813 NLM ISO Abbreviation: Eur J Hum Genet Subsets: MEDLINE

مواضيع طبية MeSH: DNA Copy Number Variations* , Genome-Wide Association Study* , Phenotype*, Alzheimer Disease/*genetics, Age of Onset ; Aged ; Aged, 80 and over ; Amyloid beta-Protein Precursor/genetics ; Amyloid beta-Protein Precursor/metabolism ; Female ; Humans ; Male ; Middle Aged ; Mutation