Mutations in FA2H in three Arab families with a clinical spectrum of neurodegeneration and hereditary spastic paraparesis.

MLA

Zaki, M. S., et al. “Mutations in FA2H in Three Arab Families with a Clinical Spectrum of Neurodegeneration and Hereditary Spastic Paraparesis.” Clinical Genetics, vol. 88, no. 1, July 2015, pp. 95–97. EBSCOhost, https://doi.org/10.1111/cge.12516.

APA

Zaki, M. S., Selim, L., Mansour, L., Mahmoud, I. G., Fenstermaker, A. G., Gabriel, S. B., & Gleeson, J. G. (2015). Mutations in FA2H in three Arab families with a clinical spectrum of neurodegeneration and hereditary spastic paraparesis. Clinical Genetics, 88(1), 95–97. https://doi.org/10.1111/cge.12516

Chicago

Zaki, M S, L Selim, L Mansour, I G Mahmoud, A G Fenstermaker, S B Gabriel, and J G Gleeson. 2015. “Mutations in FA2H in Three Arab Families with a Clinical Spectrum of Neurodegeneration and Hereditary Spastic Paraparesis.” Clinical Genetics 88 (1): 95–97. doi:10.1111/cge.12516.