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Erratum: Leigh-like syndrome due to homoplasmic m.8993t>g variant with hypocitrullinemia and unusual biochemical features suggestive of multiple carboxylase deficiency (MCD)(JIMD Reports, (2017), 33, 99-107, 10.1007/8904_2016_559)

S Balasubramaniam, B Lewis, DM Mock, HM Said, M Tarailo-Graovac, A Mattman, CD van Karnebeek, DR Thorburn, RJ Rodenburg, J Christodoulou

JIMD Reports | Published : 2017

DOI: 10.1007/8904_2017_588