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Browsing by Author Lenssen, E.W.H.

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Full TextIssue DateTitleAuthor(s)
2011NDUFA10 mutations cause complex I deficiency in a patient with Leigh diseaseHoefs, S.J.G.; Spronsen, F.J. van; Lenssen, E.W.H.; Nijtmans, L.G.J.; Rodenburg, R.J.T., et al
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