complex II deficiency

Mutations in SDHD lead to autosomal recessive encephalomyopathy and isolated mitochondrial complex II deficiency
Christopher Benjamin Jackson, Jean-Marc Nuoffer, Dagmar Hahn, Holger Prokisch, Birgit Haberberger, Matthias Gautschi, Annemarie Häberli, Sabina Gallati, André Schaller

Journal of Medical Genetics Mar 2014, 51 (3) 170-175; DOI: 10.1136/jmedgenet-2013-101932

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complex II deficiency