Effects of missense mutations and deletions on membrane anchoring and enzyme function of human steroid 21-hydroxylase (P450c21)

Biochemical and Biophysical Research Communications

Volumn 257, Issue 2, 1999, Pages 384-390

  Lajic, Svetlana ^a   Nikoshkov, Andrej ^a   Holst, Mikael ^a   Wedell, Anna ^a  

^a KAROLINSKA UNIVERSITY HOSPITAL   (Sweden)

Author keywords

Congenital adrenal hyperplasia; COS 1; In vitro transcription translation; ; Membrane anchoring; Steroid 21 hydroxylase

Indexed keywords

MUTANT PROTEIN; STEROID 21 MONOOXYGENASE;

AMINO TERMINAL SEQUENCE; ARTICLE; CASE REPORT; CONGENITAL ADRENAL HYPERPLASIA; CONTROLLED STUDY; DNA TRANSFECTION; ENZYME ACTIVITY; ENZYME POLYMORPHISM; ENZYME STRUCTURE; FEMALE; GENE DELETION; HUMAN; MEMBRANE BINDING; MICROSOME MEMBRANE; MISSENSE MUTATION; PRIORITY JOURNAL; STRUCTURE ACTIVITY RELATION;

EID: 0033551267     PISSN: 0006291X     EISSN: None     Source Type: Journal    
DOI: 10.1006/bbrc.1999.0482     Document Type: Article

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