000 01491 a2200397 4500
005 20250514073230.0
264 0 _c20040309
008 200403s 0 0 eng d
022 _a1096-7192
024 7 _a10.1016/s1096-7192(03)00087-8
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aLee, Hsien-Hsiung
245 0 0 _aDuplication of 111 bases in exon 1 of the CYP21 gene is combined with deletion of CYP21P-C4B genes in steroid 21-hydroxylase deficiency.
_h[electronic resource]
260 _bMolecular genetics and metabolism
_cJul 2003
300 _a214-20 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAdrenal Hyperplasia, Congenital
_xenzymology
650 0 4 _aAlleles
650 0 4 _aBase Sequence
650 0 4 _aComplement C4b
_xgenetics
650 0 4 _aCrossing Over, Genetic
650 0 4 _aDNA Mutational Analysis
650 0 4 _aHumans
650 0 4 _aMutation
_xgenetics
650 0 4 _aPolymerase Chain Reaction
650 0 4 _aPolymorphism, Restriction Fragment Length
650 0 4 _aRecombinant Fusion Proteins
_xgenetics
650 0 4 _aSequence Deletion
650 0 4 _aSteroid 21-Hydroxylase
_xgenetics
700 1 _aChang, Shwu-Fen
700 1 _aLo, Fu-Sung
700 1 _aChao, Hsiang-Tai
700 1 _aLin, Ching-Yu
773 0 _tMolecular genetics and metabolism
_gvol. 79
_gno. 3
_gp. 214-20
856 4 0 _uhttps://doi.org/10.1016/s1096-7192(03)00087-8
_zAvailable from publisher's website
999 _c12635699
_d12635699