Matches in Nanopublications for { ?s ?p "[Congenital adrenal hyperplasia (CAH) due to steroid 21-hydroxylase deficiency is a common inherited disorder of adrenal hormone biosynthesis due to mutations in the 21-hydroxylase gene, CYP21A2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP771657.RACC_RD8sfMaUjqfVEAd_IyKdngc6StzkUjXMNur7tLZI130_assertion description "[Congenital adrenal hyperplasia (CAH) due to steroid 21-hydroxylase deficiency is a common inherited disorder of adrenal hormone biosynthesis due to mutations in the 21-hydroxylase gene, CYP21A2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP771657.RACC_RD8sfMaUjqfVEAd_IyKdngc6StzkUjXMNur7tLZI130_provenance.