Lanoiselée, H., Nicolas, G., Wallon, D., Rovelet-Lecrux, A., Lacour, M., Rousseau, S., . . . Campion, D. (2017). APP, PSEN1, and PSEN2 mutations in early-onset Alzheimer disease: A genetic screening study of familial and sporadic cases. PLoS Med.
Chicago ZitierstilLanoiselée, Hélène-Marie, et al. "APP, PSEN1, and PSEN2 Mutations in Early-onset Alzheimer Disease: A Genetic Screening Study of Familial and Sporadic Cases." PLoS Med 2017.
MLA ZitierstilLanoiselée, Hélène-Marie, et al. "APP, PSEN1, and PSEN2 Mutations in Early-onset Alzheimer Disease: A Genetic Screening Study of Familial and Sporadic Cases." PLoS Med 2017.
Achtung: Diese Zitate sind unter Umständen nicht zu 100% korrekt.