Mitochondrial abnormalities in myofibrillar myopathies

Keyphrases

• Mitochondrial Abnormalities 100%
• Myofibrillar Myopathy 100%
• Mitochondrial DNA mutation 50%
• Mitochondrial Alterations 30%
• Long-range PCR 30%
• Late-onset 10%
• Genetic Defects 10%
• Mitochondrial Disease 10%
• Biochemical Activity 10%
• Citrate Synthase Activity 10%
• Respiratory Chain Complexes 10%
• Myofibrillar 10%
• In(III) 10%

Neuroscience

• Muscle Disorder 100%
• Mitochondrial DNA 50%
• Electron Transport Chain 10%
• Citrate Synthase 10%