000 01170 a2200349 4500
005 20250511182244.0
264 0 _c19921116
008 199211s 0 0 eng d
022 _a0141-8955
024 7 _a10.1007/BF02435977
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aGibson, K M
245 0 0 _a3-Methylglutaconyl-coenzyme-A hydratase deficiency: a new case.
_h[electronic resource]
260 _bJournal of inherited metabolic disease
_c1992
300 _a363-6 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aCarnitine
_xtherapeutic use
650 0 4 _aDiseases in Twins
650 0 4 _aFibroblasts
_xenzymology
650 0 4 _aGlutarates
_xurine
650 0 4 _aHumans
650 0 4 _aHydro-Lyases
_xdeficiency
650 0 4 _aInfant
650 0 4 _aLeucine
_xadministration & dosage
650 0 4 _aLymphocytes
_xenzymology
650 0 4 _aMale
650 0 4 _aMeglutol
_xanalogs & derivatives
700 1 _aLee, C F
700 1 _aWappner, R S
773 0 _tJournal of inherited metabolic disease
_gvol. 15
_gno. 3
_gp. 363-6
856 4 0 _uhttps://doi.org/10.1007/BF02435977
_zAvailable from publisher's website
999 _c1390099
_d1390099