Structural Characterization of Normal and Mutant Human Steroid 17α-Hydroxylase Genes: Molecular Basis of One Example of Combined 17α-Hydroxylase/17, 20 Lyase Deficiency

Molecular Endocrinology

Volumn 2, Issue 6, 1988, Pages 564-570

  Kagimoto, Masaaki ^a,c   Winter, Jeremy S D ^b   Kagimotot, Keiko ^d   Simpson, Evan R ^a   Waterman, Michael R ^a  

^a UNIVERSITY OF TEXAS SOUTHWESTERN MEDICAL CENTER   (United States)

^b UNIVERSITY OF MANITOBA   (Canada)

^c KYUSHU UNIVERSITY   (Japan)

^d KURUME UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

STEROID 17,20 LYASE; STEROID 17ALPHA MONOOXYGENASE;

CONTROLLED STUDY; HUMAN; HUMAN CELL;

ADRENAL HYPERPLASIA, CONGENITAL; ALDEHYDE-LYASES; AMINO ACID SEQUENCE; BASE SEQUENCE; CYTOCHROME P-450 ENZYME SYSTEM; DNA; DNA RESTRICTION ENZYMES; DNA, RECOMBINANT; EXONS; HUMAN; INTRONS; MOLECULAR SEQUENCE DATA; MUTATION; NUCLEIC ACID HYBRIDIZATION; STEROID 17-ALPHA-HYDROXYLASE; STEROID HYDROXYLASES; STRUCTURE-ACTIVITY RELATIONSHIP; SUPPORT, NON-U.S. GOV'T; SUPPORT, U.S. GOV'T, P.H.S.;

EID: 0023943706     PISSN: 08888809     EISSN: 19449917     Source Type: Journal    
DOI: 10.1210/mend-2-6-564     Document Type: Article

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