TY  - GEN
AU  - Küçükçongar,A
AU  - Tümer,L
AU  - Ezgü,F Süheyl
AU  - Kasapkara,Ç Seher
AU  - Jaeken,J
AU  - Matthijs,G
AU  - Rymen,D
AU  - Dalgiç,B
AU  - Bıdecı,A
AU  - Hasanoğlu,A
TI  - A case with rare type of congenital disorder of glycosylation: PGM1-CDG
SN  - 1015-8146
PY  - 2015///0619
KW  - Female
KW  - Glycogen Storage Disease
KW  - diagnosis
KW  - Humans
KW  - Infant
N1  - Publication Type: Case Reports; Letter
ER  -