Cite
Identification of novel variations in SLC6A8 and GAMT genes causing cerebral creatine deficiency syndrome.
MLA
Shen, Ming, et al. “Identification of Novel Variations in SLC6A8 and GAMT Genes Causing Cerebral Creatine Deficiency Syndrome.” Clinica Chimica Acta, vol. 532, July 2022, pp. 29–36. EBSCOhost, https://doi.org/10.1016/j.cca.2022.05.006.
APA
Shen, M., Yang, G., Chen, Z., Yang, K., Dong, H., Yin, C., Cheng, Y., Zhang, C., Gu, F., Yang, Y., & Tian, Y. (2022). Identification of novel variations in SLC6A8 and GAMT genes causing cerebral creatine deficiency syndrome. Clinica Chimica Acta, 532, 29–36. https://doi.org/10.1016/j.cca.2022.05.006
Chicago
Shen, Ming, Guangming Yang, Zhehui Chen, Kai Yang, Hui Dong, Chengliang Yin, Yuxuan Cheng, et al. 2022. “Identification of Novel Variations in SLC6A8 and GAMT Genes Causing Cerebral Creatine Deficiency Syndrome.” Clinica Chimica Acta 532 (July): 29–36. doi:10.1016/j.cca.2022.05.006.