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Severe encephalomyopathy in a patient with homoplasmic A5814G point mutation in mitochondrial tRNACys gene

✍ Scribed by Carmela Scuderi; Eugenia Borgione; Sebastiano Musumeci; Maurizio Elia; Filippa Castello; Marco Fichera; Guido Davidzon; Salvatore DiMauro

Book ID: 116792780
Publisher: Elsevier Science
Year: 2007
Tongue: English
Weight: 344 KB
Volume: 17
Category: Article
ISSN: 0960-8966
DOI: 10.1016/j.nmd.2006.11.006

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