Alerts
PDF
Other content recommended for you
- Diagnosis and therapy in neuromuscular disorders: diagnosis and new treatments in mitochondrial diseases
- Recognition, investigation and management of mitochondrial disease
- Complex I deficiency: clinical features, biochemistry and molecular genetics
- Clinical and laboratory findings in referrals for mitochondrial DNA analysis
- Mitochondrial disease: mimics and chameleons
- Clinical mitochondrial genetics
- Uncommon mutation in mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS)
- Brain imaging in mitochondrial respiratory chain deficiency: combination of brain MRI features as a useful tool for genotype/phenotype correlations
- Mitochondrial DNA polymerase γ mutations: an ever expanding molecular and clinical spectrum
- Prevalence of rare mitochondrial DNA mutations in mitochondrial disorders