Period | 19 Mar 2004 |
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Event type | Other |
Sponsor | Belgian Society for Human Genetics |
Related content
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Projects
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Hereditary and biochemical research in mitochondrial encefalomyopathies.
Project: Fundamental
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Research output
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Functional analysis of an ATP12 mutation in yeast.
Research output: Contribution to journal › Meeting abstract (Journal)
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mtDNA ananlysis in complex I deficient patients.
Research output: Contribution to journal › Meeting abstract (Journal)
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Analysis of the mitochondrial encoded subunits of complex I in 20 patients with a complex I deficiency
Research output: Contribution to journal › Article › peer-review