The Mutations Associated with Dilated Cardiomyopathy

Podobne zapisy

• D117N in Cypher/ZASP may not be a causative mutation for dilated cardiomyopathy and ventricular arrhythmias
  od: Levitas, Aviva, i wsp.
  Wydane: (2016)
• PLEKHM2 mutation leads to abnormal localization of lysosomes, impaired autophagy flux and associates with recessive dilated cardiomyopathy and left ventricular noncompaction
  od: Muhammad, Emad, i wsp.
  Wydane: (2015)
• A Novel Recessive Mutation in SPEG Causes Early Onset Dilated Cardiomyopathy
  od: Levitas, Aviva, i wsp.
  Wydane: (2020)
• Familial neonatal isolated cardiomyopathy caused by a mutation in the flavoprotein subunit of succinate dehydrogenase
  od: Levitas, Aviva, i wsp.
  Wydane: (2010)
• OBSCN Mutations Associated with Dilated Cardiomyopathy and Haploinsufficiency
  od: Marston, Steven, i wsp.
  Wydane: (2015)