000 01151 a2200325 4500
005 20250513094018.0
264 0 _c19960925
008 199609s 0 0 eng d
022 _a0022-2593
024 7 _a10.1136/jmg.33.4.295
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aSteinberg, S J
245 0 0 _aComplementation analysis in patients with the clinical phenotype of a generalised peroxisomal disorder.
_h[electronic resource]
260 _bJournal of medical genetics
_cApr 1996
300 _a295-9 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aCatalase
_xanalysis
650 0 4 _aCells, Cultured
650 0 4 _aFatty Acids
_xblood
650 0 4 _aFibroblasts
_xenzymology
650 0 4 _aGenetic Complementation Test
650 0 4 _aHumans
650 0 4 _aPeroxisomal Disorders
_xgenetics
650 0 4 _aPhenotype
650 0 4 _aPlasmalogens
_xbiosynthesis
650 0 4 _aSolubility
700 1 _aFensom, A H
773 0 _tJournal of medical genetics
_gvol. 33
_gno. 4
_gp. 295-9
856 4 0 _uhttps://doi.org/10.1136/jmg.33.4.295
_zAvailable from publisher's website
999 _c8727366
_d8727366