Matches in Nanopublications for { ?s ?p "[Steroid 21-hydroxylase deficiency is the most common enzymatic defect causing congenital adrenal hyperplasia with genotype/phenotype relationships for common mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP787615.RAAgNJQyz0rGGOQywXMk2LCpSmE_vJjgsZ7sN93ti8LM0130_assertion description "[Steroid 21-hydroxylase deficiency is the most common enzymatic defect causing congenital adrenal hyperplasia with genotype/phenotype relationships for common mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP787615.RAAgNJQyz0rGGOQywXMk2LCpSmE_vJjgsZ7sN93ti8LM0130_provenance.