Cita APA

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.

Chicago Style Citation

Cao, Siqi, et al. "Homozygous EEF1A2 Mutation Causes Dilated Cardiomyopathy, Failure to Thrive, Global Developmental Delay, Epilepsy and Early Death." Hum Mol Genet 2017.

Cita MLA

Cao, Siqi, et al. "Homozygous EEF1A2 Mutation Causes Dilated Cardiomyopathy, Failure to Thrive, Global Developmental Delay, Epilepsy and Early Death." Hum Mol Genet 2017.