Publications
- Sco2 Protein Deficiency-Based Mitochondrial Encephalomyopathy with the SMA-like Picture of Neurogenic Muscle Atrophy - Case Reports2010 | First Faculty of Medicine
- Cytochrome C oxidase deficiency in childhood2009 | First Faculty of Medicine
- Structural analysis of tissues affected by cytochrome C oxidase deficiency due to mutations in the SCO2 gene2008 | First Faculty of Medicine
- Cytochrome c oxidase deficiency due to mutations in SCO2 genePublication without faculty affiliation
- Impact of mutations in cytochrome c oxidase assembling gene SCO2 on clinical and biochemical fenotypePublication without faculty affiliation
- Clinical consequences of mutations in cytochrome c oxidase assembling gene SCO2Publication without faculty affiliation
- Cytochrome c oxidase and mutations in SCO2 genePublication without faculty affiliation
- Molecular genetic study of SCO2 gene in children with cytochrome c oxidace deficiencyPublication without faculty affiliation
- Cytochrome c oxidase deficiendy due to mutations in SCO2 genePublication without faculty affiliation
- A novel mutation in the SCO2 gene in a patient with cytochrome c oxidase deficiency and a Werdnig-Hoffmann disease phenotypePublication without faculty affiliation
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