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Mitochondrial DNA microdeletion 9204delAT in ATP6 gene in family with encephalopathy, lactic acidosis and ATP synthase deficiency : Neurogenetics
D. Fornůsková, M. Tesařová, H. Hansíková
8th Prague international symposium of child neurology.
2003 ;
() :
s. 153.
Language English Country Czech Republic
Document type Case Reports, Congress
Persistent link
https://www.medvik.cz/link/bmc03016164
- MeSH
- ATP Synthetase Complexes analysis MeSH
- Child MeSH
- Research Support as Topic MeSH
- Mitochondrial Diseases diagnosis MeSH
- DNA Mutational Analysis utilization MeSH
- Check Tag
- Child MeSH
- Male MeSH
- Publication type
- Case Reports MeSH
- Congress MeSH
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