Homozygous SPEG Mutation Is Associated With Isolated Dilated Cardiomyopathy

Antzeko izenburuak

• Striated Preferentially Expressed Protein Kinase (SPEG) in Muscle Development, Function, and Disease
  nork: Luo, Shiyu, et al.
  Argitaratua: (2021)
• A Novel Recessive Mutation in SPEG Causes Early Onset Dilated Cardiomyopathy
  nork: Levitas, Aviva, et al.
  Argitaratua: (2020)
• SPEG Interacts with Myotubularin, and Its Deficiency Causes Centronuclear Myopathy with Dilated Cardiomyopathy
  nork: Agrawal, Pankaj B., et al.
  Argitaratua: (2014)
• Striated Preferentially Expressed Protein Kinase (SPEG)-Deficient Skeletal Muscles Display Fewer Satellite Cells with Reduced Proliferation and Delayed Differentiation
  nork: Li, Qifei, et al.
  Argitaratua: (2020)
• Homozygous EEF1A2 mutation causes dilated cardiomyopathy, failure to thrive, global developmental delay, epilepsy and early death
  nork: Cao, Siqi, et al.
  Argitaratua: (2017)