000 01533 a2200445 4500
005 20250513153914.0
264 0 _c19981223
008 199812s 0 0 eng d
022 _a0002-9297
024 7 _a10.1086/302103
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aChang, C C
245 0 0 _aPhenotype-genotype relationships in complementation group 3 of the peroxisome-biogenesis disorders.
_h[electronic resource]
260 _bAmerican journal of human genetics
_cNov 1998
300 _a1294-306 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, U.S. Gov't, P.H.S.
650 0 4 _aAmino Acid Sequence
650 0 4 _aBase Sequence
650 0 4 _aCell Line
650 0 4 _aCells, Cultured
650 0 4 _aFibroblasts
_xmetabolism
650 0 4 _aGenetic Complementation Test
650 0 4 _aGenotype
650 0 4 _aHumans
650 0 4 _aIntrons
650 0 4 _aMembrane Proteins
_xbiosynthesis
650 0 4 _aMolecular Sequence Data
650 0 4 _aOligodeoxyribonucleotides
650 0 4 _aOpen Reading Frames
650 0 4 _aPeroxisomal Disorders
_xgenetics
650 0 4 _aPhenotype
650 0 4 _aPoint Mutation
650 0 4 _aPolymerase Chain Reaction
650 0 4 _aRandom Amplified Polymorphic DNA Technique
650 0 4 _aRecombinant Proteins
_xbiosynthesis
650 0 4 _aTransfection
700 1 _aGould, S J
773 0 _tAmerican journal of human genetics
_gvol. 63
_gno. 5
_gp. 1294-306
856 4 0 _uhttps://doi.org/10.1086/302103
_zAvailable from publisher's website
999 _c9757337
_d9757337