Correction: A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis.

MLA

de Boer, Elke, et al. “Correction: A MT-TL1 Variant Identified by Whole Exome Sequencing in an Individual with Intellectual Disability, Epilepsy, and Spastic Tetraparesis.” European Journal of Human Genetics : EJHG, vol. 29, no. 9, Sept. 2021, pp. 1470–71. EBSCOhost, https://doi.org/10.1038/s41431-021-00937-3.

APA

de Boer, E., Ockeloen, C. W., Matalonga, L., Horvath, R., Rodenburg, R. J., Coenen, M. J. H., Janssen, M., Henssen, D., Gilissen, C., Steyaert, W., Paramonov, I., Trimouille, A., Kleefstra, T., Verloes, A., & Vissers, L. E. L. M. (2021). Correction: A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis. European Journal of Human Genetics : EJHG, 29(9), 1470–1471. https://doi.org/10.1038/s41431-021-00937-3

Chicago

de Boer, Elke, Charlotte W Ockeloen, Leslie Matalonga, Rita Horvath, Richard J Rodenburg, Marieke J H Coenen, Mirian Janssen, et al. 2021. “Correction: A MT-TL1 Variant Identified by Whole Exome Sequencing in an Individual with Intellectual Disability, Epilepsy, and Spastic Tetraparesis.” European Journal of Human Genetics : EJHG 29 (9): 1470–71. doi:10.1038/s41431-021-00937-3.