Muhammad, E., Levitas, A., Singh, S. R., Braiman, A., Ofir, R., Etzion, S., . . . Parvari, R. (2015). PLEKHM2 mutation leads to abnormal localization of lysosomes, impaired autophagy flux and associates with recessive dilated cardiomyopathy and left ventricular noncompaction. Hum Mol Genet.
Stile di citazione ChicagoMuhammad, Emad, et al. "PLEKHM2 Mutation Leads to Abnormal Localization of Lysosomes, Impaired Autophagy Flux and Associates With Recessive Dilated Cardiomyopathy and Left Ventricular Noncompaction." Hum Mol Genet 2015.
Citazione MLAMuhammad, Emad, et al. "PLEKHM2 Mutation Leads to Abnormal Localization of Lysosomes, Impaired Autophagy Flux and Associates With Recessive Dilated Cardiomyopathy and Left Ventricular Noncompaction." Hum Mol Genet 2015.