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

Küçükçongar, A

A case with rare type of congenital disorder of glycosylation: PGM1-CDG. [electronic resource] - Genetic counseling (Geneva, Switzerland) 2015 - 87-90 p. digital

Publication Type: Case Reports; Letter

1015-8146


Female
Glycogen Storage Disease--diagnosis
Humans
Infant