Variations in the promoter ofCYP21A2gene identified in a Chinese patient with simple virilizing form of 21-hydroxylase deficiency
Author:
Publisher
Wiley
Subject
Endocrinology, Diabetes and Metabolism,Endocrinology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2265.2008.03356.x/fullpdf
Reference27 articles.
1. Congenital adrenal hyperplasia (2);White;New England Journal of Medicine,1987
2. Genetic basis of endocrine disease 2: congenital adrenal hyperplasia due to 21-hydroxylase deficiency;White;Journal of Clinical Endocrinology and Metabolism,1992
3. Disease expression and molecular genotype in congenital adrenal hyperplasia due to 21-hydroxylase deficiency;Speiser;Journal of Clinical Investigation,1992
4. Predicting phenotype in steroid 21-hydroxylase deficiency? Comprehensive genotyping in 155 unrelated, well defined patients from southern Germany;Krone;Journal of Clinical Endocrinology and Metabolism,2000
5. Steroid 21-hydroxylase deficiency: genotype may not predict phenotype;Wilson;Journal of Clinical Endocrinology and Metabolism,1995
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