A genome-wide study reveals rare CNVs exclusive to extreme phenotypes of Alzheimer disease.

MLA

Rovelet-Lecrux, Anne, et al. “A Genome-Wide Study Reveals Rare CNVs Exclusive to Extreme Phenotypes of Alzheimer Disease.” European Journal of Human Genetics, vol. 20, no. 6, June 2012, pp. 613–17. EBSCOhost, https://doi.org/10.1038/ejhg.2011.225.

APA

Rovelet-Lecrux, A., Legallic, S., Wallon, D., Flaman, J.-M., 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. (2012). A genome-wide study reveals rare CNVs exclusive to extreme phenotypes of Alzheimer disease. European Journal of Human Genetics, 20(6), 613–617. https://doi.org/10.1038/ejhg.2011.225

Chicago

Rovelet-Lecrux, Anne, Solenn Legallic, David Wallon, Jean-Michel Flaman, Olivier Martinaud, Stéphanie Bombois, Adeline Rollin-Sillaire, et al. 2012. “A Genome-Wide Study Reveals Rare CNVs Exclusive to Extreme Phenotypes of Alzheimer Disease.” European Journal of Human Genetics 20 (6): 613–17. doi:10.1038/ejhg.2011.225.