000 00986 a2200325 4500
005 20250517034335.0
264 0 _c20150619
008 201506s 0 0 eng d
022 _a1015-8146
040 _aNLM
_beng
_cNLM
100 1 _aKüçükçongar, A
245 0 0 _aA case with rare type of congenital disorder of glycosylation: PGM1-CDG.
_h[electronic resource]
260 _bGenetic counseling (Geneva, Switzerland)
_c2015
300 _a87-90 p.
_bdigital
500 _aPublication Type: Case Reports; Letter
650 0 4 _aFemale
650 0 4 _aGlycogen Storage Disease
_xdiagnosis
650 0 4 _aHumans
650 0 4 _aInfant
700 1 _aTümer, L
700 1 _aEzgü, F Süheyl
700 1 _aKasapkara, Ç Seher
700 1 _aJaeken, J
700 1 _aMatthijs, G
700 1 _aRymen, D
700 1 _aDalgiç, B
700 1 _aBıdecı, A
700 1 _aHasanoğlu, A
773 0 _tGenetic counseling (Geneva, Switzerland)
_gvol. 26
_gno. 1
_gp. 87-90
999 _c24951932
_d24951932