Cite
Mutational and haplotype map of NOTCH3 in a cohort of Italian patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)
MLA
Testi, S., et al. “Mutational and Haplotype Map of NOTCH3 in a Cohort of Italian Patients with Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL).” Journal of the Neurological Sciences, vol. 319, no. 1/2, Aug. 2012, pp. 37–41. EBSCOhost, https://doi.org/10.1016/j.jns.2012.05.025.
APA
Testi, S., Malerba, G., Ferrarini, M., Ragno, M., Pradotto, L., Mauro, A., & Fabrizi, G. M. (2012). Mutational and haplotype map of NOTCH3 in a cohort of Italian patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). Journal of the Neurological Sciences, 319(1/2), 37–41. https://doi.org/10.1016/j.jns.2012.05.025
Chicago
Testi, S., G. Malerba, M. Ferrarini, M. Ragno, L. Pradotto, A. Mauro, and G.M. Fabrizi. 2012. “Mutational and Haplotype Map of NOTCH3 in a Cohort of Italian Patients with Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL).” Journal of the Neurological Sciences 319 (1/2): 37–41. doi:10.1016/j.jns.2012.05.025.