Matches in Nanopublications for { ?s ?p "[reported 24 patients from 19 Brazilian families with 17?-hydroxylase deficiency and showed that p.W406R and p.R362C corresponded to 50% and 32% of CYP17A1 mutant alleles, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP331157.RAEemnUei2UjnvXXK6l6G1ORXub4ukx9F70RWbu5dSgdI130_assertion description "[reported 24 patients from 19 Brazilian families with 17?-hydroxylase deficiency and showed that p.W406R and p.R362C corresponded to 50% and 32% of CYP17A1 mutant alleles, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP331157.RAEemnUei2UjnvXXK6l6G1ORXub4ukx9F70RWbu5dSgdI130_provenance.
- NP874165.RAkL7RN3QkX5qW1hHVnOlzIBQ4b3UDLaE5FoQev8VGFX0130_assertion description "[reported 24 patients from 19 Brazilian families with 17?-hydroxylase deficiency and showed that p.W406R and p.R362C corresponded to 50% and 32% of CYP17A1 mutant alleles, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP874165.RAkL7RN3QkX5qW1hHVnOlzIBQ4b3UDLaE5FoQev8VGFX0130_provenance.
- NP344642.RA71R5bXrFaSB1FN_tCYc0U0tkCEDv05P2Hj3Bdj4jFck130_assertion description "[reported 24 patients from 19 Brazilian families with 17?-hydroxylase deficiency and showed that p.W406R and p.R362C corresponded to 50% and 32% of CYP17A1 mutant alleles, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP344642.RA71R5bXrFaSB1FN_tCYc0U0tkCEDv05P2Hj3Bdj4jFck130_provenance.