Cao, S., Smith, L. L., Padilla-Lopez, S. R., Guida, B. S., Blume, E., Shi, J., . . . Agrawal, P. B. (2017). Homozygous EEF1A2 mutation causes dilated cardiomyopathy, failure to thrive, global developmental delay, epilepsy and early death. Hum Mol Genet.
Citação norma ChicagoCao, Siqi, et al. "Homozygous EEF1A2 Mutation Causes Dilated Cardiomyopathy, Failure to Thrive, Global Developmental Delay, Epilepsy and Early Death." Hum Mol Genet 2017.
Citação norma MLACao, Siqi, et al. "Homozygous EEF1A2 Mutation Causes Dilated Cardiomyopathy, Failure to Thrive, Global Developmental Delay, Epilepsy and Early Death." Hum Mol Genet 2017.
Nota: a formatação da citação pode não corresponder 100% ao definido pela respectiva norma.