000 01203 a2200361 4500
005 20250512233856.0
264 0 _c19830610
008 198306s 0 0 eng d
022 _a0141-8955
024 7 _a10.1007/BF01800004
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aVan Leeuwen, G H
245 0 0 _aCell genetic studies on propionyl-CoA carboxylase deficient cell lines.
_h[electronic resource]
260 _bJournal of inherited metabolic disease
_c1982
300 _a115-20 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aCarboxy-Lyases
_xdeficiency
650 0 4 _aCell Fusion
650 0 4 _aCell Line
650 0 4 _aFemale
650 0 4 _aFibroblasts
_xcytology
650 0 4 _aGenetic Complementation Test
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMethylmalonyl-CoA Decarboxylase
650 0 4 _aPropionates
_xmetabolism
700 1 _aDe Vrieze, G
700 1 _aGimpel, J A
700 1 _aHuisjes, H J
700 1 _aHommes, F A
773 0 _tJournal of inherited metabolic disease
_gvol. 5
_gno. 2
_gp. 115-20
856 4 0 _uhttps://doi.org/10.1007/BF01800004
_zAvailable from publisher's website
999 _c6820165
_d6820165