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Browsing by Author Carrozzo, R.

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Full TextIssue DateTitleAuthor(s)
2009Dystonia and deafness due to SUCLA2 defect; Clinical course and biochemical markers in 16 children.Morava, E.; Steuerwald, U.; Carrozzo, R.; Kluijtmans, L.A.J.; Joensen, F., et al
2007SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness.Carrozzo, R.; Dionisi-Vici, C.; Steuerwald, U.; Lucioli, S.; Deodato, F., et al
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