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Browsing by Author Carrozzo, R.
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| Full Text | Issue Date | Title | Author(s) | | 2009 | Dystonia 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 |
| 2007 | SUCLA2 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 |
Showing results 1 to 2 of 2
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