Infantile cardioencephalopathy due to a COX15 gene defect: report and review. [electronic resource]
Producer: 20110830Description: 840-4 p. digitalISSN:- 1552-4833
- Brain -- pathology
- Brain Diseases, Metabolic, Inborn -- diagnosis
- Cytochrome-c Oxidase Deficiency -- diagnosis
- Electron Transport Chain Complex Proteins -- metabolism
- Electron Transport Complex IV -- genetics
- Female
- Heart Diseases -- diagnosis
- Humans
- Infant, Newborn
- Magnetic Resonance Imaging
- Mutation -- genetics
- Myocardium -- pathology
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Publication Type: Case Reports; Journal Article; Review
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