000 01238 a2200349 4500
005 20250514205635.0
264 0 _c20050505
008 200505s 0 0 eng d
022 _a0141-8955
024 7 _a10.1023/B:BOLI.0000045768.38073.22
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aKölker, S
245 0 0 _aChallenges for basic research in glutaryl-CoA dehydrogenase deficiency.
_h[electronic resource]
260 _bJournal of inherited metabolic disease
_c2004
300 _a843-9 p.
_bdigital
500 _aPublication Type: Journal Article; Review
650 0 4 _aAmino Acid Metabolism, Inborn Errors
_xpathology
650 0 4 _aAnimals
650 0 4 _aGlutarates
_xmetabolism
650 0 4 _aGlutaryl-CoA Dehydrogenase
650 0 4 _aHumans
650 0 4 _aNeostriatum
_xpathology
650 0 4 _aNeurons
_xpathology
650 0 4 _aOxidoreductases Acting on CH-CH Group Donors
_xdeficiency
700 1 _aStrauss, K A
700 1 _aGoodman, S I
700 1 _aHoffmann, G F
700 1 _aOkun, J G
700 1 _aKoeller, D M
773 0 _tJournal of inherited metabolic disease
_gvol. 27
_gno. 6
_gp. 843-9
856 4 0 _uhttps://doi.org/10.1023/B:BOLI.0000045768.38073.22
_zAvailable from publisher's website
999 _c15194443
_d15194443