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APA Citation
Falk, M. J., Gai, X., Shigematsu, M., Vilardo, E., Takase, R., McCormick, E., Christian, T., Place, E., Pierce, E. A., Consugar, M., Gamper, H. B., Rossmanith, W., & Hou, Y. (2016). a novel HSD17B10 mutation impairing the activities of the mitochondrial RNase P complex causes X-linked intractable epilepsy and neurodevelopmental regression. RNA biology, 13(5), 477–485. http://access.bl.uk/ark:/81055/vdc_100033828360.0x000026