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 |