Chol, M., Lebon, S., Benit, P., Chretien, D., de Lonlay, P., Goldenberg, A., . . . Munnich, A. (2003). The mitochondrial DNA G13513A MELAS mutation in the NADH dehydrogenase 5 gene is a frequent cause of Leigh-like syndrome with isolated complex I deficiency. BMJ Group.
Citação norma ChicagoChol, M., et al. The Mitochondrial DNA G13513A MELAS Mutation in the NADH Dehydrogenase 5 Gene Is a Frequent Cause of Leigh-like Syndrome With Isolated Complex I Deficiency. BMJ Group, 2003.
Citação norma MLAChol, M., et al. The Mitochondrial DNA G13513A MELAS Mutation in the NADH Dehydrogenase 5 Gene Is a Frequent Cause of Leigh-like Syndrome With Isolated Complex I Deficiency. BMJ Group, 2003.
Nota: a formatação da citação pode não corresponder 100% ao definido pela respectiva norma.