| 000 | 01643 a2200457 4500 | ||
|---|---|---|---|
| 005 | 20250513090018.0 | ||
| 264 | 0 | _c19960529 | |
| 008 | 199605s 0 0 eng d | ||
| 022 | _a0021-9738 | ||
| 024 | 7 |
_a10.1172/JCI118465 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aPaton, B C | |
| 245 | 0 | 0 |
_aOxidation of pristanic acid in fibroblasts and its application to the diagnosis of peroxisomal beta-oxidation defects. _h[electronic resource] |
| 260 |
_bThe Journal of clinical investigation _cFeb 1996 |
||
| 300 |
_a681-8 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 |
_a3-Hydroxyacyl CoA Dehydrogenases _xdeficiency |
| 650 | 0 | 4 |
_aAustralia _xepidemiology |
| 650 | 0 | 4 |
_aBile Acids and Salts _xblood |
| 650 | 0 | 4 | _aCells, Cultured |
| 650 | 0 | 4 |
_aEnoyl-CoA Hydratase _xdeficiency |
| 650 | 0 | 4 |
_aFatty Acids _xblood |
| 650 | 0 | 4 |
_aFibroblasts _xmetabolism |
| 650 | 0 | 4 | _aGenetic Complementation Test |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aHybrid Cells |
| 650 | 0 | 4 | _aIsomerases |
| 650 | 0 | 4 |
_aMicrobodies _xchemistry |
| 650 | 0 | 4 |
_aMultienzyme Complexes _xdeficiency |
| 650 | 0 | 4 | _aOxidation-Reduction |
| 650 | 0 | 4 | _aPeroxisomal Bifunctional Enzyme |
| 650 | 0 | 4 |
_aPeroxisomal Disorders _xdiagnosis |
| 650 | 0 | 4 |
_aPhytanic Acid _xmetabolism |
| 650 | 0 | 4 | _aPrenatal Diagnosis |
| 650 | 0 | 4 |
_aZellweger Syndrome _xdiagnosis |
| 700 | 1 | _aSharp, P C | |
| 700 | 1 | _aCrane, D I | |
| 700 | 1 | _aPoulos, A | |
| 773 | 0 |
_tThe Journal of clinical investigation _gvol. 97 _gno. 3 _gp. 681-8 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1172/JCI118465 _zAvailable from publisher's website |
| 999 |
_c8608269 _d8608269 |
||