Prevalence of common mutations in the CYP17A1 gene in Chinese Han population
Author:
Publisher
Elsevier BV
Subject
Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine
Reference23 articles.
1. 17-hydroxylation deficiency in man;Biglieri;J Clin Invest,1966
2. Male pseudohermaphroditism due to 17 alpha-hydroxylase deficiency;New;J Clin Invest,1970
3. Regional mapping of genes encoding human steroidogenic enzymes: P450scc to 15q23–q24, adrenodoxin to 11q22; adrenodoxin reductase to 17q24–q25; and P450c17 to 10q24–q25;Sparkes;DNA Cell Biol,1991
4. Localization of the human CYP17 gene (cytochrome P450(17 alpha)) to 10q24.3 by fluorescence in situ hybridization and simultaneous chromosome banding;Fan;Genomics,1992
5. Two prevalent CYP17 mutations and genotype–phenotype correlations in 24 Brazilian patients with 17-hydroxylase deficiency;Costa-Santos;J Clin Endocrinol Metab,2004
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