The mitochondrial 13513G>A mutation is most frequent in Leigh syndrome combined with reduced complex I activity, optic atrophy and/or Wolff–Parkinson–White

✍ Scribed by Ruiter, E Mariken; Siers, Marloes H; van den Elzen, Christa; van Engelen, Baziel G; Smeitink, Jan A M; Rodenburg, Richard J; Hol, Frans A

• Book ID: 110026836
• Publisher: Nature Publishing Group
• Year: 2006
• Tongue: English
• Weight: 206 KB
• Volume: 15
• Category: Article
• ISSN: 1018-4813
• DOI: 10.1038/sj.ejhg.5201735