A single amino acid substitution in the putative redox partner-binding site of P450c17 as cause of isolated 17,20-lyase deficiency

Journal of Clinical Endocrinology and Metabolism

Volumn 82, Issue 11, 1997, Pages 3807-3812

  Biason Lauber, A ^a   Leiberman, E ^b   Zachmann, M ^a  

^a Department of Pediatrics   (Switzerland)

^b BEN GURION UNIVERSITY OF THE NEGEV   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

CYTOCHROME P450; STEROID 17,20 LYASE;

ALLELE; AMINO ACID SUBSTITUTION; ARTICLE; BASE PAIRING; BINDING SITE; CASE REPORT; CRYPTORCHISM; ENZYME DEFICIENCY; ENZYME ISOLATION; GENE DELETION; GENE REARRANGEMENT; HUMAN; MALE; MICROPENIS; NEWBORN; OXIDATION REDUCTION REACTION; PRIORITY JOURNAL; PROTEIN PROCESSING;

RAPHIA FRATER;

EID: 0030694398     PISSN: 0021972X     EISSN: None     Source Type: Journal    
DOI: 10.1210/jc.82.11.3807     Document Type: Article

References (17)

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2. Deleted in proof.
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