Description of clinical features and genetic analysis of one ultra-rare (SPG64) and two common forms (SPG5A and SPG15) of hereditary spastic paraplegia families.

MLA

Pashaei, Mahdieh, et al. “Description of Clinical Features and Genetic Analysis of One Ultra-Rare (SPG64) and Two Common Forms (SPG5A and SPG15) of Hereditary Spastic Paraplegia Families.” Journal of Neurogenetics, vol. 35, no. 2, June 2021, pp. 84–94. EBSCOhost, https://doi.org/10.1080/01677063.2021.1895146.

APA

Pashaei, M., Davarzani, A., Hajati, R., Zamani, B., Nafissi, S., Larti, F., Nilipour, Y., Rohani, M., & Alavi, A. (2021). Description of clinical features and genetic analysis of one ultra-rare (SPG64) and two common forms (SPG5A and SPG15) of hereditary spastic paraplegia families. Journal of Neurogenetics, 35(2), 84–94. https://doi.org/10.1080/01677063.2021.1895146

Chicago

Pashaei, Mahdieh, Atefeh Davarzani, Reza Hajati, Babak Zamani, Shahriar Nafissi, Farzaneh Larti, Yalda Nilipour, Mohammad Rohani, and Afagh Alavi. 2021. “Description of Clinical Features and Genetic Analysis of One Ultra-Rare (SPG64) and Two Common Forms (SPG5A and SPG15) of Hereditary Spastic Paraplegia Families.” Journal of Neurogenetics 35 (2): 84–94. doi:10.1080/01677063.2021.1895146.