Truncating mutation in intracellular phospholipase A1 gene (DDHD2) in hereditary spastic paraplegia with intellectual disability (SPG54).

MLA

Alrayes, Nuha, et al. “Truncating Mutation in Intracellular Phospholipase A1 Gene (DDHD2) in Hereditary Spastic Paraplegia with Intellectual Disability (SPG54).” BMC Research Notes, vol. 8, no. 1, June 2015, pp. 1–5. EBSCOhost, https://doi.org/10.1186/s13104-015-1227-4.

APA

Alrayes, N., Mohamoud, H. S. A., Jelani, M., Ahmad, S., Vadgama, N., Bakur, K., Simpson, M., Al-Aama, J. Y., & Nasir, J. (2015). Truncating mutation in intracellular phospholipase A1 gene (DDHD2) in hereditary spastic paraplegia with intellectual disability (SPG54). BMC Research Notes, 8(1), 1–5. https://doi.org/10.1186/s13104-015-1227-4

Chicago

Alrayes, Nuha, Hussein Sheikh Ali Mohamoud, Musharraf Jelani, Saleem Ahmad, Nirmal Vadgama, Khadijah Bakur, Michael Simpson, Jumana Yousuf Al-Aama, and Jamal Nasir. 2015. “Truncating Mutation in Intracellular Phospholipase A1 Gene (DDHD2) in Hereditary Spastic Paraplegia with Intellectual Disability (SPG54).” BMC Research Notes 8 (1): 1–5. doi:10.1186/s13104-015-1227-4.