Cao, S., Smith, L.L., Padilla-Lopez, S.R., Guida, B.S., Blume, E., Shi, J., Morton, S.U., Brownstein, C.A., Beggs, A.H., Kruer, M.C., Agrawal, P.B. (2017) Homozygous EEF1A2 mutation causes dilated cardiomyopathy, failure to thrive, global developmental delay, epilepsy and early death. Human molecular genetics. 26:3545-3552

Cao, S., Smith, L.L., Padilla-Lopez, S.R., Guida, B.S., Blume, E., Shi, J., Morton, S.U., Brownstein, C.A., Beggs, A.H., Kruer, M.C., Agrawal, P.B. (2017) Homozygous EEF1A2 mutation causes dilated cardiomyopathy, failure to thrive, global developmental delay, epilepsy and early death. Human molecular genetics. 26:3545-3552