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G.P.3.07 Novel mutation in SUCLA2 gene: Encephalomyopathy, dystonia and deafness associated with mild methylmalonic aciduria and mtDNA depletions

✍ Scribed by A.E.N. Nascimento Osorio; A.N.S. Navarro-Sastre; J.C. Colomer; C.P. Paredes; A.G. Gutierrez; C.O. Ortez; M.V. Vilaseca; J.M. Montoya; T.R. Ribes

Book ID: 116793972
Publisher: Elsevier Science
Year: 2009
Tongue: English
Weight: 41 KB
Volume: 19
Category: Article
ISSN: 0960-8966
DOI: 10.1016/j.nmd.2009.06.065

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