Two novel CYP11B1 mutations in congenital adrenal hyperplasia due to steroid 11β hydroxylase deficiency in a Tunisian family
published in: General and Comparative Endocrinology
date of publication: 2011-12-22
main subject: congenital disorder, congenital adrenal hyperplasia
Cites articles 17
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Article - wd:Q38901898