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 |