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Browsing by Author Martin, M.A.

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Full TextIssue DateTitleAuthor(s)
2008Mitochondrial DNA background modulates the assembly kinetics of OXPHOS complexes in a cellular model of mitochondrial disease.Pello, R.; Martin, M.A.; Carelli, V.; Nijtmans, L.G.J.; Achilli, A., et al
2007X-linked NDUFA1 gene mutations associated with mitochondrial encephalomyopathy.Fernandez-Moreira, D.; Ugalde, C.; Smeets, R.; Rodenburg, R.J.T.; Lopez-Laso, E., et al
2004Molecular analysis of myophosphorylase deficiency in Dutch patients with McArdle's disease.Martin, M.A.; Rubio, J.C.; Wevers, R.A.; Engelen, B.G.M. van; Steenbergen-Spanjers, G.C.H., et al
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