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