MtDNA mutations are a common cause of severe disease phenotypes in children with Leigh syndrome

✍ Scribed by Karin Naess; Christoph Freyer; Helene Bruhn; Rolf Wibom; Gunilla Malm; Inger Nennesmo; Ulrika von Döbeln; Nils-Göran Larsson

• Book ID: 113484344
• Publisher: Elsevier Science
• Year: 2009
• Tongue: English
• Weight: 345 KB
• Volume: 1787
• Category: Article
• ISSN: 0005-2728
• DOI: 10.1016/j.bbabio.2008.11.014