Mitochondrial G8292A and C8794T mutations in patients with Niemann-Pick disease type C.

MLA

Maserrat, Shahin, et al. “Mitochondrial G8292A and C8794T Mutations in Patients with Niemann-Pick Disease Type C.” Biomedical Reports, vol. 9, no. 1, July 2018, pp. 65–73. EBSCOhost, https://doi.org/10.3892/br.2018.1095.

APA

Maserrat, S., Sharifpanah, F., Akbari, L., Tonekaboni, S. H., Karimzadeh, P., Asharafi, M. R., Mazrouei, S., Sauer, H., & Houshmand, M. (2018). Mitochondrial G8292A and C8794T mutations in patients with Niemann-Pick disease type C. Biomedical Reports, 9(1), 65–73. https://doi.org/10.3892/br.2018.1095

Chicago

Maserrat, Shahin, Fatemeh Sharifpanah, Leila Akbari, Seyed Hasan Tonekaboni, Parvaneh Karimzadeh, Mahmood Reza Asharafi, Safoura Mazrouei, Heinrich Sauer, and Massoud Houshmand. 2018. “Mitochondrial G8292A and C8794T Mutations in Patients with Niemann-Pick Disease Type C.” Biomedical Reports 9 (1): 65–73. doi:10.3892/br.2018.1095.