Mitochondrial myopathy and ophthalmoplegia in a sporadic patient with the G12315A mutation in mitochondrial DNA

✍ Scribed by Charalampos L Karadimas; Leonardo Salviati; Sabrina Sacconi; Penelope Chronopoulou; Sara Shanske; Eduardo Bonilla; Darryl C De Vivo; Salvatore DiMauro

• Book ID: 117669593
• Publisher: Elsevier Science
• Year: 2002
• Tongue: English
• Weight: 77 KB
• Volume: 12
• Category: Article
• ISSN: 0960-8966
• DOI: 10.1016/s0960-8966(02)00072-x