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1. PLEKHM2 mutation leads to abnormal localization of lysosomes, impaired autophagy flux and associates with recessive dilated cardiomyopathy and left ventricular noncompaction

   1. Muhammad, Emad
   2. Levitas, Avita
   3. Levitas, Avita
   4. Singh, Sonia
   5. Braiman, Alex
   6. Ofir, Rivka
   7. Etzion, Sharon

   2016 - Forschungsinformationssystem des UKE - frei zugänglich