Mutations of the hexose-6-phosphate dehydrogenase gene rarely cause hyperandrogenemic polycystic ovary syndrome

Steroids

Volumn 76, Issue 1-2, 2011, Pages 135-139

  Qin, Kenan ^a   Rosenfield, Robert L ^a  

^a UNIVERSITY OF CHICAGO   (United States)

Author keywords

Cortisone reductase deficiency; Hexose 6 phosphate gene variants; Polycystic ovary syndrome

Indexed keywords

DNA; GLUCOSE 6 PHOSPHATE DEHYDROGENASE;

ARTICLE; CODON; CONTROLLED STUDY; DNA SEQUENCE; EXON; FEMALE; GENE DELETION; GENE FREQUENCY; GENE LINKAGE DISEQUILIBRIUM; GENE MUTATION; GENETIC VARIABILITY; GENOTYPE; HUMAN; HYPERANDROGENISM; MAJOR CLINICAL STUDY; MISSENSE MUTATION; NUCLEOTIDE SEQUENCE; OVARY POLYCYSTIC DISEASE; POLYMERASE CHAIN REACTION; RESTRICTION FRAGMENT LENGTH POLYMORPHISM;

ANIMALS; CARBOHYDRATE DEHYDROGENASES; FEMALE; GENETIC VARIATION; GENOTYPE; HUMANS; HYPERANDROGENISM; MUTATION, MISSENSE; POLYCYSTIC OVARY SYNDROME;

EID: 78650512109     PISSN: 0039128X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.steroids.2010.10.001     Document Type: Article

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