Cardiomyopathy associated with neurologic disorders and mitochondrial phenotype. [electronic resource]
Producer: 20030314Description: 759-65 p. digitalISSN:- 0883-0738
- Adolescent
- Cardiomyopathies -- genetics
- Child
- Child, Preschool
- DNA, Mitochondrial
- Dystonia -- pathology
- Electron Transport Complex I
- Female
- Friedreich Ataxia -- pathology
- Gene Deletion
- Humans
- Infant
- Infant, Newborn
- Kearns-Sayre Syndrome -- pathology
- Leigh Disease -- pathology
- Male
- Mitochondria -- genetics
- Mitochondrial Myopathies -- genetics
- Muscle, Skeletal -- pathology
- Mutation
- Myocardium -- pathology
- NADH, NADPH Oxidoreductases -- metabolism
- Neuromuscular Diseases -- pathology
- Ophthalmoplegia -- pathology
- Phenotype
- Seizures -- pathology
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Publication Type: Journal Article
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