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. 2017 Oct 27;33:111. doi: 10.1007/8904_2017_588

Erratum: Leigh-Like Syndrome Due to Homoplasmic m.8993T>G Variant with Hypocitrullinemia and Unusual Biochemical Features Suggestive of Multiple Carboxylase Deficiency (MCD)

Eva Morava 1,, Matthias Baumgartner 2, Marc Patterson 3, Shamima Rahman 4, Johannes Zschocke 5, Verena Peters 6
PMCID: PMC5669218  PMID: 29076057

Erratum to: JIMD Reports DOI: 10.1007/8904_2016_559

Errata to:

Chapter 559: Leigh-Like Syndrome Due to Homoplasmic m.8993T>G Variant with Hypocitrullinemia and Unusual Biochemical Features Suggestive of Multiple Carboxylase Deficiency (MCD), doi: 10.1007/8904_2016_559

Shanti Balasubramaniam, B. Lewis, D.M. Mock, H.M. Said, M. Tarailo-Graovac, A. Mattman, C.D. van Karnebeek, D.R. Thorburn, R.J. Rodenburg, and J. Christodoulou

The publisher regrets to inform that one of the author name was incorrect. The correct name is C.D. van Karnebeek (wrong: C.D. van Karneebek).

Footnotes

The updated original online versions of the original chapters can be found under DOI 10.1007/8904_2016_559

Contributor Information

Collaborators: Matthias R. Baumgartner, Marc Patterson, Shamima Rahman, Verena Peters, Eva Morava, and Johannes Zschocke


Articles from JIMD Reports are provided here courtesy of Wiley

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