APA
Le Ber I., Van Bortel I., Nicolas G., Bouya-Ahmed K., Camuzat A., Wallon D., De Septenville A., Latouche M., Lattante S., Kabashi E., Jornea L., Hannequin D. & Brice A. (20140929). hnRNPA2B1 and hnRNPA1 mutations are rare in patients with "multisystem proteinopathy" and frontotemporal lobar degeneration phenotypes. : Neurobiology of aging.
Chicago
Le Ber Isabelle, Van Bortel Inge, Nicolas Gael, Bouya-Ahmed Kawtar, Camuzat Agnès, Wallon David, De Septenville Anne, Latouche Morwena, Lattante Serena, Kabashi Edor, Jornea Ludmila, Hannequin Didier and Brice Alexis. 20140929. hnRNPA2B1 and hnRNPA1 mutations are rare in patients with "multisystem proteinopathy" and frontotemporal lobar degeneration phenotypes. : Neurobiology of aging.
Harvard
Le Ber I., Van Bortel I., Nicolas G., Bouya-Ahmed K., Camuzat A., Wallon D., De Septenville A., Latouche M., Lattante S., Kabashi E., Jornea L., Hannequin D. and Brice A. (20140929). hnRNPA2B1 and hnRNPA1 mutations are rare in patients with "multisystem proteinopathy" and frontotemporal lobar degeneration phenotypes. : Neurobiology of aging.
MLA
Le Ber Isabelle, Van Bortel Inge, Nicolas Gael, Bouya-Ahmed Kawtar, Camuzat Agnès, Wallon David, De Septenville Anne, Latouche Morwena, Lattante Serena, Kabashi Edor, Jornea Ludmila, Hannequin Didier and Brice Alexis. hnRNPA2B1 and hnRNPA1 mutations are rare in patients with "multisystem proteinopathy" and frontotemporal lobar degeneration phenotypes. : Neurobiology of aging. 20140929.