000 01304 a2200397 4500
005 20250513183830.0
264 0 _c19990712
008 199907s 0 0 eng d
022 _a1096-7192
024 7 _a10.1006/mgme.1999.2862
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aMallolas, J
245 0 0 _aBiochemical phenotype and its relationship with genotype in hyperphenylalaninemia heterozygotes.
_h[electronic resource]
260 _bMolecular genetics and metabolism
_cJun 1999
300 _a156-61 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aFemale
650 0 4 _aGenetic Carrier Screening
650 0 4 _aGenotype
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMutation
650 0 4 _aPhenotype
650 0 4 _aPhenylalanine
_xblood
650 0 4 _aPhenylalanine Hydroxylase
_xdeficiency
650 0 4 _aPhenylketonurias
_xblood
650 0 4 _aReference Values
650 0 4 _aTyrosine
_xblood
700 1 _aMilĂ , M
700 1 _aLambruschini, N
700 1 _aCambra, F J
700 1 _aCampistol, J
700 1 _aVilaseca, M A
773 0 _tMolecular genetics and metabolism
_gvol. 67
_gno. 2
_gp. 156-61
856 4 0 _uhttps://doi.org/10.1006/mgme.1999.2862
_zAvailable from publisher's website
999 _c10314937
_d10314937