000 | 01621 a2200457 4500 | ||
---|---|---|---|
005 | 20250511181430.0 | ||
264 | 0 | _c19921218 | |
008 | 199212s 0 0 eng d | ||
022 | _a0361-7742 | ||
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aYokota, I | |
245 | 0 | 0 |
_aThe molecular basis of medium chain acyl-CoA dehydrogenase deficiency: survey and evolution of 985A----G transition, and identification of five rare types of mutation within the medium chain acyl-CoA dehydrogenase gene. _h[electronic resource] |
260 |
_bProgress in clinical and biological research _c1992 |
||
300 |
_a425-40 p. _bdigital |
||
500 | _aPublication Type: Journal Article | ||
650 | 0 | 4 | _aAcyl-CoA Dehydrogenase |
650 | 0 | 4 |
_aAcyl-CoA Dehydrogenases _xdeficiency |
650 | 0 | 4 |
_aAdenine _xphysiology |
650 | 0 | 4 | _aAlleles |
650 | 0 | 4 | _aBase Sequence |
650 | 0 | 4 | _aBiological Evolution |
650 | 0 | 4 | _aCells, Cultured |
650 | 0 | 4 |
_aEthnicity _xgenetics |
650 | 0 | 4 |
_aFibroblasts _xphysiology |
650 | 0 | 4 |
_aGenetic Variation _xgenetics |
650 | 0 | 4 |
_aGuanine _xphysiology |
650 | 0 | 4 | _aHomozygote |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 |
_aMetabolism, Inborn Errors _xenzymology |
650 | 0 | 4 | _aMolecular Sequence Data |
650 | 0 | 4 |
_aMutation _xgenetics |
650 | 0 | 4 | _aPolymerase Chain Reaction |
650 | 0 | 4 | _aPolymorphism, Restriction Fragment Length |
650 | 0 | 4 | _aSkin Physiological Phenomena |
650 | 0 | 4 | _aSurveys and Questionnaires |
700 | 1 | _aCoates, P M | |
700 | 1 | _aHale, D E | |
700 | 1 | _aRinaldo, P | |
700 | 1 | _aTanaka, K | |
773 | 0 |
_tProgress in clinical and biological research _gvol. 375 _gp. 425-40 |
|
999 |
_c1366062 _d1366062 |