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Clinical variability in neurohepatic syndrome due to combined mitochondrial DNA depletion and Gaucher disease.
Harvengt, Julie; Wanty, Catherine; De Paepe, Boel; Sempoux, Christine; Revencu, Nicole; Smet, Joél; Van Coster, Rudy; Lissens, Willy; Seneca, Sara; Weekers, Laurent; Sokal, Etienne; Debray, François-Guillaume.
Afiliação
  • Harvengt J; Metabolic Unit, Department of Medical Genetics, CHU-CHC, Liège, Belgium.
  • Wanty C; Liver Unit, Department of Pediatrics, Cliniques Universitaires Saint-Luc, Brussels, Belgium.
  • De Paepe B; Department of Pediatrics, Division of Pediatric Neurology and Metabolism, Ghent University Hospital, Ghent, Belgium.
  • Sempoux C; Department of pathology, Cliniques Universitaires Saint-Luc, Brussels, Belgium.
  • Revencu N; Department of Medical Genetics, Cliniques Universitaires Saint-Luc, Brussels, Belgium.
  • Smet J; Department of Pediatrics, Division of Pediatric Neurology and Metabolism, Ghent University Hospital, Ghent, Belgium.
  • Van Coster R; Department of Pediatrics, Division of Pediatric Neurology and Metabolism, Ghent University Hospital, Ghent, Belgium.
  • Lissens W; Department of Medical Genetics, University Hospital AZ-VUB, Brussels, Belgium.
  • Seneca S; Department of Medical Genetics, University Hospital AZ-VUB, Brussels, Belgium.
  • Weekers L; Metabolic Unit, Department of Medical Genetics, CHU-CHC, Liège, Belgium.
  • Sokal E; Liver Unit, Department of Pediatrics, Cliniques Universitaires Saint-Luc, Brussels, Belgium.
  • Debray FG; Metabolic Unit, Department of Medical Genetics, CHU-CHC, Liège, Belgium.
Mol Genet Metab Rep ; 1: 223-231, 2014.
Article em En | MEDLINE | ID: mdl-27896091

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Mol Genet Metab Rep Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Bélgica

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Mol Genet Metab Rep Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Bélgica