A novel mitochondrial DNA mutation in COX1 leads to strokes, seizures, and lactic acidosis. [electronic resource]
Producer: 20090813Description: 328-34 p. digitalISSN:- 1439-1899
- Acidosis, Lactic -- diagnosis
- Alleles
- Cerebral Infarction -- diagnosis
- Child
- DNA Mutational Analysis
- DNA, Mitochondrial -- genetics
- Electron Transport Complex IV -- genetics
- Epilepsy, Tonic-Clonic -- diagnosis
- Female
- Histidine -- genetics
- Humans
- Learning Disabilities -- diagnosis
- MELAS Syndrome -- diagnosis
- Magnesium -- metabolism
- Psychomotor Disorders -- diagnosis
- Sequence Analysis, DNA
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
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