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Glycogen Storage Disease Type IV: A Rare Cause for Neuromuscular Disorders or Often Missed?
Schene, Imre F; Korenke, Christoph G; Huidekoper, Hidde H; van der Pol, Ludo; Dooijes, Dennis; Breur, Johannes M P J; Biskup, Saskia; Fuchs, Sabine A; Visser, Gepke.
Afiliação
  • Schene IF; Department of Metabolic Diseases, Wilhelmina Children's Hospital, University Medical Centre Utrecht, Utrecht, The Netherlands.
  • Korenke CG; Department of Neuropediatrics, Children's Hospital Klinikum Oldenburg, Oldenburg, Germany.
  • Huidekoper HH; Department of Pediatrics, Center for Lysosomal and Metabolic Diseases, Erasmus Medical Center, Rotterdam, The Netherlands.
  • van der Pol L; Department of Neurology, University Medical Centre Utrecht, Utrecht, The Netherlands.
  • Dooijes D; Department of Medical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Breur JMPJ; Department of Pediatric Cardiology, Wilhelmina Children's Hospital, University Medical Centre Utrecht, Utrecht, The Netherlands.
  • Biskup S; CeGaT GmbH and Praxis für Humangenetik Tübingen, Tübingen, Germany.
  • Fuchs SA; Department of Metabolic Diseases, Wilhelmina Children's Hospital, University Medical Centre Utrecht, Utrecht, The Netherlands.
  • Visser G; Department of Metabolic Diseases, Wilhelmina Children's Hospital, University Medical Centre Utrecht, Utrecht, The Netherlands. G.Visser-4@umcutrecht.nl.
JIMD Rep ; 45: 99-104, 2019.
Article em En | MEDLINE | ID: mdl-30569318
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: JIMD Rep Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Holanda País de publicação: Estados Unidos
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: JIMD Rep Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Holanda País de publicação: Estados Unidos