000 01483 a2200409 4500
005 20250514205635.0
264 0 _c20050505
008 200505s 0 0 eng d
022 _a0141-8955
024 7 _a10.1023/B:BOLI.0000045766.98718.d6
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aMühlhausen, C
245 0 0 _aVascular dysfunction as an additional pathomechanism in glutaric aciduria type I.
_h[electronic resource]
260 _bJournal of inherited metabolic disease
_c2004
300 _a829-34 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't; Review
650 0 4 _aAmino Acid Metabolism, Inborn Errors
_xgenetics
650 0 4 _aAnimals
650 0 4 _aBrain Diseases
_xpathology
650 0 4 _aCerebrovascular Circulation
_xphysiology
650 0 4 _aGlutarates
_xurine
650 0 4 _aGlutaryl-CoA Dehydrogenase
650 0 4 _aHumans
650 0 4 _aOligonucleotide Array Sequence Analysis
650 0 4 _aOxidoreductases Acting on CH-CH Group Donors
_xdeficiency
650 0 4 _aVascular Diseases
_xgenetics
700 1 _aErgün, S
700 1 _aStrauss, K A
700 1 _aKoeller, D M
700 1 _aCrnic, L
700 1 _aWoontner, M
700 1 _aGoodman, S I
700 1 _aUllrich, K
700 1 _aBraulke, T
773 0 _tJournal of inherited metabolic disease
_gvol. 27
_gno. 6
_gp. 829-34
856 4 0 _uhttps://doi.org/10.1023/B:BOLI.0000045766.98718.d6
_zAvailable from publisher's website
999 _c15194442
_d15194442