The mitochondrial 13513G>A mutation is most frequent in Leigh syndrome combined with reduced complex I activity, optic atrophy and/or Wolff–Parkinson–White
Ruiter, E Mariken, Siers, Marloes H, van den Elzen, Christa, van Engelen, Baziel G, Smeitink, Jan A M, Rodenburg, Richard J, Hol, Frans AVolume:
15
Year:
2006
Language:
english
Pages:
7
DOI:
10.1038/sj.ejhg.5201735
File:
PDF, 206 KB
english, 2006