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Keyword [Leigh syndrome]
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1. The Mechanism Of Clinical And Genetic Heterogeneity And Compensatory Metabolic Re-programming In Mitochondrial Diseases
2. Clinical And Whole Genetic Analysis Of Mitochondrial Encephalomyopathy
3. The Heterogeneity Of Genotype And Phenotype In Mitochondrial Encephalopathy
4. A mutation in cytochrome c oxidase subunit VIa causes defective L-type calcium currents and Leigh syndrome-like phenotypes in Drosophila
5. Clinical And Genetic Analysis Of 7 Cases Of Mitochondrial Diseases
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