000 01438 a2200433 4500
005 20250513134152.0
264 0 _c19980210
008 199802s 0 0 eng d
022 _a0340-6199
024 7 _a10.1007/s004310050746
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aCohen, L H
245 0 0 _aGrowth failure, encephalopathy, and endocrine dysfunctions in two siblings, one with 5-oxoprolinase deficiency.
_h[electronic resource]
260 _bEuropean journal of pediatrics
_cDec 1997
300 _a935-8 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aBrain Diseases
_xenzymology
650 0 4 _aConsanguinity
650 0 4 _aEndocrine System Diseases
_xenzymology
650 0 4 _aFemale
650 0 4 _aGrowth Disorders
_xenzymology
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aMetabolism, Inborn Errors
_xenzymology
650 0 4 _aPhenotype
650 0 4 _aPyroglutamate Hydrolase
_xdeficiency
650 0 4 _aSyndrome
700 1 _aVamos, E
700 1 _aHeinrichs, C
700 1 _aToppet, M
700 1 _aCourtens, W
700 1 _aKumps, A
700 1 _aMardens, Y
700 1 _aCarlsson, B
700 1 _aGrillner, L
700 1 _aLarsson, A
773 0 _tEuropean journal of pediatrics
_gvol. 156
_gno. 12
_gp. 935-8
856 4 0 _uhttps://doi.org/10.1007/s004310050746
_zAvailable from publisher's website
999 _c9422483
_d9422483