Homozygous SPEG Mutation Is Associated With Isolated Dilated Cardiomyopathy

समान संसाधन

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