APA (7th ed.) Citation

Li, X., Li, L., Sun, Y., Lv, F., Zhang, G., Liu, W., . . . Liu, S. (2019). Whole exome sequencing reveals two novel compound heterozygous mutations in TWNK as a cause of the hepatocerebral form of mitochondrial DNA depletion syndrome: A case report. BMC.

Chicago Style (17th ed.) Citation

Li, Xianghong, Liangshan Li, Yaqi Sun, Fuyan Lv, Guoqing Zhang, Wenmiao Liu, Meiyan Zhang, Hong Jiang, and Shiguo Liu. Whole Exome Sequencing Reveals Two Novel Compound Heterozygous Mutations in TWNK as a Cause of the Hepatocerebral Form of Mitochondrial DNA Depletion Syndrome: A Case Report. BMC, 2019.

MLA (9th ed.) Citation

Li, Xianghong, et al. Whole Exome Sequencing Reveals Two Novel Compound Heterozygous Mutations in TWNK as a Cause of the Hepatocerebral Form of Mitochondrial DNA Depletion Syndrome: A Case Report. BMC, 2019.