Pitfalls in characterizing P450c17 mutations associated with isolated 17,20-lyase deficiency

Journal of Clinical Endocrinology and Metabolism

Volumn 86, Issue 9, 2001, Pages 4416-4423

  Gupta, Manisha K ^a   Geller, David H ^b   Auchus, Richard J ^a,c  

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

^b CEDARS SINAI MEDICAL CENTER   (United States)

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

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; CYTOCHROME B5; CYTOCHROME P450; CYTOCHROME P450 REDUCTASE; CYTOCHROME P450C17; PRASTERONE; STEROID 17,20 LYASE; STEROID 17ALPHA MONOOXYGENASE; UNCLASSIFIED DRUG;

ADRENAL GLAND; AMINO ACID SUBSTITUTION; ANIMAL CELL; ARTICLE; BINDING SITE; COMPUTER MODEL; CONTROLLED STUDY; DIAGNOSTIC ACCURACY; ENZYME ACTIVE SITE; ENZYME DEFICIENCY; GENE ISOLATION; GENE MAPPING; GENE MUTATION; GENETIC ASSOCIATION; GONAD FUNCTION; MICROSOME; NONHUMAN; OXIDATION REDUCTION REACTION; PHENOTYPE; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN PROTEIN INTERACTION; REPRODUCIBILITY; YEAST;

ANIMALIA;

EID: 0034840366     PISSN: 0021972X     EISSN: None     Source Type: Journal    
DOI: 10.1210/jcem.86.9.7812     Document Type: Article

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