The genetic and functional basis of isolated 17, 20-lyase deficiency

Nature Genetics

Volumn 17, Issue 2, 1997, Pages 201-205

  Geller, David H ^a   Auchus, Richard J ^a   Mendonça, Berenice B ^b   Miller, Walter L ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF SÃO PAULO   (Brazil)

Author keywords

[No Author keywords available]

Indexed keywords

PRIMER DNA; STEROID 17ALPHA MONOOXYGENASE;

ADOLESCENT; ANIMAL; ARTICLE; BINDING SITE; CASE REPORT; CELL STRAIN COS1; CHEMICAL STRUCTURE; CONGENITAL ADRENAL HYPERPLASIA; GENETIC TRANSFECTION; GENETICS; HOMOZYGOTE; HUMAN; INFANT; MALE; METABOLISM; MUTATION; NUCLEOTIDE SEQUENCE; OXIDATION REDUCTION REACTION; POLYMERASE CHAIN REACTION; PROTEIN CONFORMATION;

ADOLESCENT; ADRENAL HYPERPLASIA, CONGENITAL; ANIMALS; BASE SEQUENCE; BINDING SITES; COS CELLS; DNA PRIMERS; HOMOZYGOTE; HUMANS; INFANT; MALE; MODELS, MOLECULAR; MUTATION; OXIDATION-REDUCTION; POLYMERASE CHAIN REACTION; PROTEIN CONFORMATION; STEROID 17-ALPHA-HYDROXYLASE; TRANSFECTION;

EID: 0031252385     PISSN: 10614036     EISSN: 15461718     Source Type: Journal    
DOI: 10.1038/ng1097-201     Document Type: Letter

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