Falk, M. J., Gai, X., Shigematsu, M., Vilardo, E., Takase, R., McCormick, E., . . . 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 Biol.
Citación estilo ChicagoFalk, Marni J., et al. "A Novel HSD17B10 Mutation Impairing the Activities of the Mitochondrial RNase P Complex Causes X-linked Intractable Epilepsy and Neurodevelopmental Regression." RNA Biol 2016.
Cita MLAFalk, Marni J., et al. "A Novel HSD17B10 Mutation Impairing the Activities of the Mitochondrial RNase P Complex Causes X-linked Intractable Epilepsy and Neurodevelopmental Regression." RNA Biol 2016.
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