Cite
tRNA methyltransferase homolog gene TRMT10A mutation in young onset diabetes and primary microcephaly in humans.
MLA
Igoillo-Esteve, Mariana, et al. “TRNA Methyltransferase Homolog Gene TRMT10A Mutation in Young Onset Diabetes and Primary Microcephaly in Humans.” PLoS Genetics, vol. 9, no. 10, Oct. 2013, p. e1003888. EBSCOhost, https://doi.org/10.1371/journal.pgen.1003888.
APA
Igoillo-Esteve, M., Genin, A., Lambert, N., Désir, J., Pirson, I., Abdulkarim, B., Simonis, N., Drielsma, A., Marselli, L., Marchetti, P., Vanderhaeghen, P., Eizirik, D. L., Wuyts, W., Julier, C., Chakera, A. J., Ellard, S., Hattersley, A. T., Abramowicz, M., & Cnop, M. (2013). tRNA methyltransferase homolog gene TRMT10A mutation in young onset diabetes and primary microcephaly in humans. PLoS Genetics, 9(10), e1003888. https://doi.org/10.1371/journal.pgen.1003888
Chicago
Igoillo-Esteve, Mariana, Anne Genin, Nelle Lambert, Julie Désir, Isabelle Pirson, Baroj Abdulkarim, Nicolas Simonis, et al. 2013. “TRNA Methyltransferase Homolog Gene TRMT10A Mutation in Young Onset Diabetes and Primary Microcephaly in Humans.” PLoS Genetics 9 (10): e1003888. doi:10.1371/journal.pgen.1003888.