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