000 01645 a2200493 4500
005 20250514064533.0
264 0 _c20040108
008 200401s 0 0 eng d
022 _a1096-7192
024 7 _a10.1016/s1096-7192(03)00034-9
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aNagan, Narasimhan
245 0 0 _aThe frequency of short-chain acyl-CoA dehydrogenase gene variants in the US population and correlation with the C(4)-acylcarnitine concentration in newborn blood spots.
_h[electronic resource]
260 _bMolecular genetics and metabolism
_cApr 2003
300 _a239-46 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aAlleles
650 0 4 _aButyryl-CoA Dehydrogenase
_xdeficiency
650 0 4 _aCarnitine
_xanalogs & derivatives
650 0 4 _aExons
650 0 4 _aFatty Acids
_xmetabolism
650 0 4 _aGene Frequency
650 0 4 _aGenetic Variation
650 0 4 _aGenetics, Population
650 0 4 _aGenotype
650 0 4 _aHeterozygote
650 0 4 _aHomozygote
650 0 4 _aHumans
650 0 4 _aInfant, Newborn
650 0 4 _aMass Screening
650 0 4 _aMass Spectrometry
650 0 4 _aMutation
650 0 4 _aPhenotype
650 0 4 _aScattering, Radiation
650 0 4 _aTemperature
650 0 4 _aUnited States
700 1 _aKruckeberg, Kent E
700 1 _aTauscher, Angela L
700 1 _aBailey, Karen Snow
700 1 _aRinaldo, Piero
700 1 _aMatern, Dietrich
773 0 _tMolecular genetics and metabolism
_gvol. 78
_gno. 4
_gp. 239-46
856 4 0 _uhttps://doi.org/10.1016/s1096-7192(03)00034-9
_zAvailable from publisher's website
999 _c12497821
_d12497821