Cite
Matchmaking facilitates the diagnosis of an autosomal-recessive mitochondrial disease caused by biallelic mutation of the tRNA isopentenyltransferase (TRIT1) gene.
MLA
Kernohan, Kristin D., et al. “Matchmaking Facilitates the Diagnosis of an Autosomal-Recessive Mitochondrial Disease Caused by Biallelic Mutation of the TRNA Isopentenyltransferase (TRIT1) Gene.” Human Mutation, vol. 38, no. 5, May 2017, pp. 511–16. EBSCOhost, https://doi.org/10.1002/humu.23196.
APA
Kernohan, K. D., Dyment, D. A., Pupavac, M., Cramer, Z., McBride, A., Bernard, G., Straub, I., Tetreault, M., Hartley, T., Huang, L., Sell, E., Majewski, J., Rosenblatt, D. S., Shoubridge, E., Mhanni, A., Myers, T., Proud, V., Vergano, S., Spangler, B., … Thiffault, I. (2017). Matchmaking facilitates the diagnosis of an autosomal-recessive mitochondrial disease caused by biallelic mutation of the tRNA isopentenyltransferase (TRIT1) gene. Human Mutation, 38(5), 511–516. https://doi.org/10.1002/humu.23196
Chicago
Kernohan, Kristin D, David A Dyment, Mihaela Pupavac, Zvi Cramer, Arran McBride, Genevieve Bernard, Isabella Straub, et al. 2017. “Matchmaking Facilitates the Diagnosis of an Autosomal-Recessive Mitochondrial Disease Caused by Biallelic Mutation of the TRNA Isopentenyltransferase (TRIT1) Gene.” Human Mutation 38 (5): 511–16. doi:10.1002/humu.23196.