| Period | 6 Sep 2005 → 9 Sep 2005 |
|---|---|
| Event type | Conference |
| Sponsor | SSIEM |
| Location | Paris, France |
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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Biochemical and molecular studies, and prenatal diagnosis in a family with methylmalonic aciduria due to cob(I)alamin adenosyltransferase deficiency.
Research output: Contribution to journal › Meeting abstract (Journal)
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Functional analysis of a human atp12 mutation in yeast S. cerevisiae.
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
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Denaturating high performance liquid chromatography, a rapid mutation screening technique for the entire mitochondrial genome.
Research output: Contribution to journal › Meeting abstract (Journal)