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SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness

✍ Scribed by 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.

Book ID: 121695156
Publisher: Oxford University Press
Year: 2007
Tongue: English
Weight: 773 KB
Volume: 130
Category: Article
ISSN: 0006-8950
DOI: 10.1093/brain/awl389

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