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Title
The mitochondrial 13513G > A mutation is most frequent in Leigh syndrome combined with reduced complex I activity, optic atrophy and/or Wolff-Parkinson-White.
Authors
Ruiter EM; Siers MH; van den Elzen C; van Engelen BG; Smeitink JA; Rodenburg RJ; Hol FA
Publication
European journal of human genetics : EJHG, 2007, Vol 15, Issue 2, p155