A case with rare type of congenital disorder of glycosylation: PGM1-CDG

Genet Couns. 2015;26(1):87-90.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Female
  • Glycogen Storage Disease / diagnosis*
  • Glycogen Storage Disease / pathology
  • Glycogen Storage Disease / physiopathology
  • Humans
  • Infant

Supplementary concepts

  • Glycogen Storage Disease XIV