Congenital disorder of glycosylation type Ia: Heterogeneity in the clinical presentation from multivisceral failure to hyperinsulinaemic hypoglycaemia as leading symptoms in three infants with phosphomannomutase deficiency Journal Articles uri icon

Overview

Authors

Published in

  • Journal of Inherited Metabolic Disease

Time

Date/time value

  • 2009

Identity

Digital Object Identifier (DOI)

  • 10.1007/s10545-009-1180-2

Additional Document Info

Parent Title

  • JOURNAL OF INHERITED METABOLIC DISEASE

Volume

  • 32

Issue

  • 1

Publisher

  • Kluwer Academic Publishers