Phenotypic variability in familial prion diseases due to the D178N mutation.

MLA

Zarranz, J. J., et al. “Phenotypic Variability in Familial Prion Diseases Due to the D178N Mutation.” Journal of Neurology, Neurosurgery, and Psychiatry, vol. 76, no. 11, Nov. 2005, pp. 1491–96. EBSCOhost, https://doi.org/10.1136/jnnp.2004.056606.

APA

Zarranz, J. J., Digon, A., Atarés, B., Rodríguez-Martínez, A. B., Arce, A., Carrera, N., Fernández-Manchola, I., Fernández-Martínez, M., Fernández-Maiztegui, C., Forcadas, I., Galdos, L., Gómez-Esteban, J. C., Ibáñez, A., Lezcano, E., López de Munain, A., Martí-Massó, J. F., Mendibe, M. M., Urtasun, M., Uterga, J. M., … de Pancorbo, M. M. (2005). Phenotypic variability in familial prion diseases due to the D178N mutation. Journal of Neurology, Neurosurgery, and Psychiatry, 76(11), 1491–1496. https://doi.org/10.1136/jnnp.2004.056606

Chicago

Zarranz, J J, A Digon, B Atarés, A B Rodríguez-Martínez, A Arce, N Carrera, I Fernández-Manchola, et al. 2005. “Phenotypic Variability in Familial Prion Diseases Due to the D178N Mutation.” Journal of Neurology, Neurosurgery, and Psychiatry 76 (11): 1491–96. doi:10.1136/jnnp.2004.056606.