LRRK2 haplotype-sharing analysis in Parkinson's disease reveals a novel p.S1761R mutation.

MLA

Lorenzo-Betancor, Oswaldo, et al. “LRRK2 Haplotype-Sharing Analysis in Parkinson’s Disease Reveals a Novel p.S1761R Mutation.” Movement Disorders : Official Journal of the Movement Disorder Society, vol. 27, no. 1, Jan. 2012, pp. 146–51. EBSCOhost, https://doi.org/10.1002/mds.23968.

APA

Lorenzo-Betancor, O., Samaranch, L., Ezquerra, M., Tolosa, E., Lorenzo, E., Irigoyen, J., Gaig, C., Pastor, M. A., Soto-Ortolaza, A. I., Ross, O. A., Rodríguez-Oroz, M. C., Valldeoriola, F., Martí, M. J., Luquin, M. R., Perez-Tur, J., Burguera, J. A., Obeso, J. A., & Pastor, P. (2012). LRRK2 haplotype-sharing analysis in Parkinson’s disease reveals a novel p.S1761R mutation. Movement Disorders : Official Journal of the Movement Disorder Society, 27(1), 146–151. https://doi.org/10.1002/mds.23968

Chicago

Lorenzo-Betancor, Oswaldo, Lluís Samaranch, Mario Ezquerra, Eduardo Tolosa, Elena Lorenzo, Jaione Irigoyen, Carles Gaig, et al. 2012. “LRRK2 Haplotype-Sharing Analysis in Parkinson’s Disease Reveals a Novel p.S1761R Mutation.” Movement Disorders : Official Journal of the Movement Disorder Society 27 (1): 146–51. doi:10.1002/mds.23968.