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

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

doi:10.1007/8904_2017_588

Shanti Balasubramaniam^13,14,15,
B. Lewis¹⁶,
D. M. Mock¹⁷,
H. M. Said¹⁸,
M. Tarailo-Graovac¹⁹,
A. Mattman²⁰,
C. D. van Karnebeek²¹,
D. R. Thorburn^22,23,
R. J. Rodenburg²⁴ &
…
J. Christodoulou^22,23

Part of the book series: JIMD Reports ((JIMD,volume 33))

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

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Erratum to: JIMD Reports DOI: 10.1007/8904_2016_559

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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).

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Authors and Affiliations

Metabolic Unit, Department of Rheumatology and Metabolic Medicine, Princess Margaret Hospital, Perth, WA, Australia
Shanti Balasubramaniam
School of Paediatrics and Child Health, University of Western Australia, Perth, WA, Australia
Shanti Balasubramaniam
Western Sydney Genetics Program, Children’s Hospital at Westmead, Westmead, NSW, Australia
Shanti Balasubramaniam
PathWest Laboratories WA, Princess Margaret Hospital, Perth, WA, Australia
B. Lewis
Department of Biochemistry and Molecular Biology, University of Arkansas for Medical Sciences, Little Rock, AR, USA
D. M. Mock
Department of Medicine, University of California School of Medicine Irvine, Irvine, CA, USA
H. M. Said
Centre for Molecular Medicine, Department of Medical Genetics, Child and Family Research Institute, University of British Columbia, Vancouver, BC, Canada
M. Tarailo-Graovac
Adult Metabolic Diseases Clinic, Division of Endocrinology and Metabolism, Vancouver General Hospital, UBC, Vancouver, BC, Canada
A. Mattman
Centre for Molecular Medicine, Department of Pediatrics, Child and Family Research Institute, University of British Columbia, Vancouver, BC, Canada
C. D. van Karnebeek
Murdoch Childrens Research Institute and Victorian Clinical Genetics Services, Royal Children’s Hospital, Melbourne, VIC, Australia
D. R. Thorburn & J. Christodoulou
Department of Paediatrics, The University of Melbourne, Melbourne, VIC, Australia
D. R. Thorburn & J. Christodoulou
Radboud Center for Mitochondrial Medicine, Radboud University Medical Centre, Nijmegen, The Netherlands
R. J. Rodenburg

Authors

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

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Editors and Affiliations

Tulane University Medical School, New Orleans, Louisiana, USA
Eva Morava (Editor-in-Chief) (Editor-in-Chief)
Division of Metabolism and Children’s Research Centre, University Children’s Hospital Zurich, Zurich, Switzerland
Matthias Baumgartner
Division of Child and Adolescent Neurology, Mayo Clinic, Rochester, Minnesota, USA
Marc Patterson
Clinical and Molecular Genetics Unit, UCL Institute of Child Health, London, UK
Shamima Rahman
Division of Human Genetics, Medical University Innsbruck, Innsbruck, Austria
Johannes Zschocke
Center for Child and Adolescent Medicine, Heidelberg University Hospital, Heidelberg, Germany
Verena Peters (Managing Editor) (Managing Editor)

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Balasubramaniam, S. et al. (2017). Erratum: Leigh-Like Syndrome Due to Homoplasmic m.8993T>G Variant with Hypocitrullinemia and Unusual Biochemical Features Suggestive of Multiple Carboxylase Deficiency (MCD). In: Morava, E., Baumgartner, M., Patterson, M., Rahman, S., Zschocke, J., Peters, V. (eds) JIMD Reports, Volume 33. JIMD Reports, vol 33. Springer, Berlin, Heidelberg. https://doi.org/10.1007/8904_2017_588

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DOI: https://doi.org/10.1007/8904_2017_588
Publisher Name: Springer, Berlin, Heidelberg
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