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) Books uri icon

Overview

Published in

  • Journal of Inherited Metabolic Disease Reports

Time

Date/time value

  • 2017

Identity

Digital Object Identifier (DOI)

  • 10.1007/8904_2017_588

Additional Document Info

Parent Title

  • JIMD Reports

Volume

  • 33

Publisher

  • Springer