Matches in Nanopublications for { ?s ?p "[Congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency is a common autosomal recessive disorder caused by mutations in the steroid 21-hydroxylase gene (CYP21A2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency is a common autosomal recessive disorder caused by mutations in the steroid 21-hydroxylase gene (CYP21A2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency is a common autosomal recessive disorder caused by mutations in the steroid 21-hydroxylase gene (CYP21A2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1021738.RAfT5Bsq2vpoEZEYhDx-vEkwFiqEdT5t5Te-r9eP-w_kk130_assertion description "[Congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency is a common autosomal recessive disorder caused by mutations in the steroid 21-hydroxylase gene (CYP21A2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1021738.RAfT5Bsq2vpoEZEYhDx-vEkwFiqEdT5t5Te-r9eP-w_kk130_provenance.
- NP1021735.RAoasLKaq0kKTeqsiBnYchsQBu-BI-8QeN_ghWNA6LXpI130_assertion description "[Congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency is a common autosomal recessive disorder caused by mutations in the steroid 21-hydroxylase gene (CYP21A2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1021735.RAoasLKaq0kKTeqsiBnYchsQBu-BI-8QeN_ghWNA6LXpI130_provenance.
- NP1021737.RA52XmMisdFI7POBwj9aJF9O-eYjAln5hGWsrz3rk7eJs130_assertion description "[Congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency is a common autosomal recessive disorder caused by mutations in the steroid 21-hydroxylase gene (CYP21A2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1021737.RA52XmMisdFI7POBwj9aJF9O-eYjAln5hGWsrz3rk7eJs130_provenance.