Expression of the human genes for steroid 21-hydroxylase and its C169R mutant in insect cells and functional analysis of the expression products
Author:
Publisher
Pleiades Publishing Ltd
Subject
Structural Biology,Biophysics
Link
http://link.springer.com/content/pdf/10.1134/S0026893307010098.pdf
Reference35 articles.
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3. Wedell A., Luthman H. 1993. Steroid 21-hydroxylase deficiency: Two additional mutations in salt-wasting disease and rapid screening of disease-causing mutations. Hum. Mol. Genet. 2, 499–504.
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5. Krone N., Braun A., Roscher A.A., Knorr D., Schwarz H.P. 2000. Predicting phenotype in steroid 21-hydroxylase deficiency? Comprehensive genotyping in 155 unrelated, well defined patients from Southern Germany. J. Clin. Endocrinol. Metab. 85, 1059–1065.
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