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SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness
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| Zeitschriftentitel: | Brain |
|---|---|
| Personen und Körperschaften: | , , , , , , , , , , , , , , , , , , |
| In: | Brain, 130, 2007, 3, S. 862-874 |
| Format: | E-Article |
| Sprache: | Englisch |
| veröffentlicht: |
Oxford University Press (OUP)
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| Schlagwörter: |
| author_facet |
Carrozzo, R. Dionisi-Vici, C. Steuerwald, U. Lucioli, S. Deodato, F. Di Giandomenico, S. Bertini, E. Franke, B. Kluijtmans, L. A. J. Meschini, M. C. Rizzo, C. Piemonte, F. Rodenburg, R. Santer, R. Santorelli, F. M. van Rooij, A. Vermunt-de Koning, D. Morava, E. Wevers, R. A. Carrozzo, R. Dionisi-Vici, C. Steuerwald, U. Lucioli, S. Deodato, F. Di Giandomenico, S. Bertini, E. Franke, B. Kluijtmans, L. A. J. Meschini, M. C. Rizzo, C. Piemonte, F. Rodenburg, R. Santer, R. Santorelli, F. M. van Rooij, A. Vermunt-de Koning, D. Morava, E. Wevers, R. A. |
|---|---|
| author |
Carrozzo, R. Dionisi-Vici, C. Steuerwald, U. Lucioli, S. Deodato, F. Di Giandomenico, S. Bertini, E. Franke, B. Kluijtmans, L. A. J. Meschini, M. C. Rizzo, C. Piemonte, F. Rodenburg, R. Santer, R. Santorelli, F. M. van Rooij, A. Vermunt-de Koning, D. Morava, E. Wevers, R. A. |
| spellingShingle |
Carrozzo, R. Dionisi-Vici, C. Steuerwald, U. Lucioli, S. Deodato, F. Di Giandomenico, S. Bertini, E. Franke, B. Kluijtmans, L. A. J. Meschini, M. C. Rizzo, C. Piemonte, F. Rodenburg, R. Santer, R. Santorelli, F. M. van Rooij, A. Vermunt-de Koning, D. Morava, E. Wevers, R. A. Brain SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness Neurology (clinical) |
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carrozzo, r. |
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Carrozzo, R. Dionisi-Vici, C. Steuerwald, U. Lucioli, S. Deodato, F. Di Giandomenico, S. Bertini, E. Franke, B. Kluijtmans, L. A. J. Meschini, M. C. Rizzo, C. Piemonte, F. Rodenburg, R. Santer, R. Santorelli, F. M. van Rooij, A. Vermunt-de Koning, D. Morava, E. Wevers, R. A. 0006-8950 1460-2156 Oxford University Press (OUP) Neurology (clinical) http://dx.doi.org/10.1093/brain/awl389 SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness Brain |
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| title |
SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness |
| title_unstemmed |
SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness |
| title_full |
SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness |
| title_fullStr |
SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness |
| title_full_unstemmed |
SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness |
| title_short |
SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness |
| title_sort |
sucla2 mutations are associated with mild methylmalonic aciduria, leigh-like encephalomyopathy, dystonia and deafness |
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Neurology (clinical) |
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http://dx.doi.org/10.1093/brain/awl389 |
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| author | Carrozzo, R., Dionisi-Vici, C., Steuerwald, U., Lucioli, S., Deodato, F., Di Giandomenico, S., Bertini, E., Franke, B., Kluijtmans, L. A. J., Meschini, M. C., Rizzo, C., Piemonte, F., Rodenburg, R., Santer, R., Santorelli, F. M., van Rooij, A., Vermunt-de Koning, D., Morava, E., Wevers, R. A. |
| author_facet | Carrozzo, R., Dionisi-Vici, C., Steuerwald, U., Lucioli, S., Deodato, F., Di Giandomenico, S., Bertini, E., Franke, B., Kluijtmans, L. A. J., Meschini, M. C., Rizzo, C., Piemonte, F., Rodenburg, R., Santer, R., Santorelli, F. M., van Rooij, A., Vermunt-de Koning, D., Morava, E., Wevers, R. A., Carrozzo, R., Dionisi-Vici, C., Steuerwald, U., Lucioli, S., Deodato, F., Di Giandomenico, S., Bertini, E., Franke, B., Kluijtmans, L. A. J., Meschini, M. C., Rizzo, C., Piemonte, F., Rodenburg, R., Santer, R., Santorelli, F. M., van Rooij, A., Vermunt-de Koning, D., Morava, E., Wevers, R. A. |
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| spelling | Carrozzo, R. Dionisi-Vici, C. Steuerwald, U. Lucioli, S. Deodato, F. Di Giandomenico, S. Bertini, E. Franke, B. Kluijtmans, L. A. J. Meschini, M. C. Rizzo, C. Piemonte, F. Rodenburg, R. Santer, R. Santorelli, F. M. van Rooij, A. Vermunt-de Koning, D. Morava, E. Wevers, R. A. 0006-8950 1460-2156 Oxford University Press (OUP) Neurology (clinical) http://dx.doi.org/10.1093/brain/awl389 SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness Brain |
| spellingShingle | Carrozzo, R., Dionisi-Vici, C., Steuerwald, U., Lucioli, S., Deodato, F., Di Giandomenico, S., Bertini, E., Franke, B., Kluijtmans, L. A. J., Meschini, M. C., Rizzo, C., Piemonte, F., Rodenburg, R., Santer, R., Santorelli, F. M., van Rooij, A., Vermunt-de Koning, D., Morava, E., Wevers, R. A., Brain, SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness, Neurology (clinical) |
| title | SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness |
| title_full | SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness |
| title_fullStr | SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness |
| title_full_unstemmed | SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness |
| title_short | SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness |
| title_sort | sucla2 mutations are associated with mild methylmalonic aciduria, leigh-like encephalomyopathy, dystonia and deafness |
| title_unstemmed | SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness |
| topic | Neurology (clinical) |
| url | http://dx.doi.org/10.1093/brain/awl389 |