The mitochondrial 13513G>A mutation is most frequent in Leigh syndrome combined with reduced complex I activity, optic atrophy and/or Wolff–Parkinson–White (Q62671329)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | The mitochondrial 13513G>A mutation is most frequent in Leigh syndrome combined with reduced complex I activity, optic atrophy and/or Wolff–Parkinson–White |
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The mitochondrial 13513G > A mutation is most frequent in Leigh syndrome combined with reduced complex I activity, optic atrophy and/or Wolff-Parkinson-White (English)
E Mariken Ruiter
Marloes H Siers
Christa van den Elzen
Baziel G van Engelen
Jan A M Smeitink
15 November 2006