LRP10 genetic variants in familial Parkinson's disease and dementia with Lewy bodies: a genome-wide linkage and sequencing study.

MLA

Quadri, Marialuisa, et al. “LRP10 Genetic Variants in Familial Parkinson’s Disease and Dementia with Lewy Bodies: A Genome-Wide Linkage and Sequencing Study.” The Lancet. Neurology, vol. 17, no. 7, July 2018, pp. 597–608. EBSCOhost, https://doi.org/10.1016/S1474-4422(18)30179-0.

APA

Quadri, M., Mandemakers, W., Grochowska, M. M., Masius, R., Geut, H., Fabrizio, E., Breedveld, G. J., Kuipers, D., Minneboo, M., Vergouw, L. J. M., Carreras Mascaro, A., Yonova-Doing, E., Simons, E., Zhao, T., Di Fonzo, A. B., Chang, H.-C., Parchi, P., Melis, M., Correia Guedes, L., … Bonifati, V. (2018). LRP10 genetic variants in familial Parkinson’s disease and dementia with Lewy bodies: a genome-wide linkage and sequencing study. The Lancet. Neurology, 17(7), 597–608. https://doi.org/10.1016/S1474-4422(18)30179-0

Chicago

Quadri, Marialuisa, Wim Mandemakers, Martyna M Grochowska, Roy Masius, Hanneke Geut, Edito Fabrizio, Guido J Breedveld, et al. 2018. “LRP10 Genetic Variants in Familial Parkinson’s Disease and Dementia with Lewy Bodies: A Genome-Wide Linkage and Sequencing Study.” The Lancet. Neurology 17 (7): 597–608. doi:10.1016/S1474-4422(18)30179-0.