000 01712 a2200457 4500
005 20250514004343.0
264 0 _c20011204
008 200112s 0 0 eng d
022 _a0014-2972
024 7 _a10.1046/j.1365-2362.2001.00877.x
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aVan Veldhoven, P P
245 0 0 _aFibroblast studies documenting a case of peroxisomal 2-methylacyl-CoA racemase deficiency: possible link between racemase deficiency and malabsorption and vitamin K deficiency.
_h[electronic resource]
260 _bEuropean journal of clinical investigation
_cAug 2001
300 _a714-22 p.
_bdigital
500 _aPublication Type: Case Reports; Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aCells, Cultured
650 0 4 _aFatty Acids
_xchemical synthesis
650 0 4 _aFemale
650 0 4 _aFibroblasts
_xenzymology
650 0 4 _aHumans
650 0 4 _aInfant, Newborn
650 0 4 _aIsomerism
650 0 4 _aMalabsorption Syndromes
_xetiology
650 0 4 _aOxidation-Reduction
650 0 4 _aPalmitic Acids
_xchemical synthesis
650 0 4 _aPeroxisomal Disorders
_xenzymology
650 0 4 _aPeroxisomes
_xenzymology
650 0 4 _aRacemases and Epimerases
_xdeficiency
650 0 4 _aSkin
_xcytology
650 0 4 _aVitamin K Deficiency
_xetiology
700 1 _aMeyhi, E
700 1 _aSquires, R H
700 1 _aFransen, M
700 1 _aFournier, B
700 1 _aBrys, V
700 1 _aBennett, M J
700 1 _aMannaerts, G P
773 0 _tEuropean journal of clinical investigation
_gvol. 31
_gno. 8
_gp. 714-22
856 4 0 _uhttps://doi.org/10.1046/j.1365-2362.2001.00877.x
_zAvailable from publisher's website
999 _c11400987
_d11400987