Matches in Nanopublications for { ?s ?p "[Our findings document that patients carrying these SCAD gene variations may develop clinically relevant SCAD deficiency, and that patients with even mild ethylmalonic aciduria should be tested for these variations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Our findings document that patients carrying these SCAD gene variations may develop clinically relevant SCAD deficiency, and that patients with even mild ethylmalonic aciduria should be tested for these variations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP229197.RAk0S3CdaEl3lSxne9cgQCVT0_jY6riAP_9-68t6RZyiw130_assertion description "[Our findings document that patients carrying these SCAD gene variations may develop clinically relevant SCAD deficiency, and that patients with even mild ethylmalonic aciduria should be tested for these variations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP229197.RAk0S3CdaEl3lSxne9cgQCVT0_jY6riAP_9-68t6RZyiw130_provenance.
- NP1743.RAZJ2iQE0T19qnF1vY3k2b9vPwI_vzA4aQ4fxDfzVAiyg130_assertion description "[Our findings document that patients carrying these SCAD gene variations may develop clinically relevant SCAD deficiency, and that patients with even mild ethylmalonic aciduria should be tested for these variations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1743.RAZJ2iQE0T19qnF1vY3k2b9vPwI_vzA4aQ4fxDfzVAiyg130_provenance.
- NP220373.RA1KAimQQEmKUZ2trfj--iosNz6grGLcF1x4zbXaRmUuw130_assertion description "[Our findings document that patients carrying these SCAD gene variations may develop clinically relevant SCAD deficiency, and that patients with even mild ethylmalonic aciduria should be tested for these variations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP220373.RA1KAimQQEmKUZ2trfj--iosNz6grGLcF1x4zbXaRmUuw130_provenance.
- NP1193.RAJJfnP1wtHzgNlJSvkbzB-7dYHENBGxHnxACcnsu8sr8130_assertion description "[Our findings document that patients carrying these SCAD gene variations may develop clinically relevant SCAD deficiency, and that patients with even mild ethylmalonic aciduria should be tested for these variations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1193.RAJJfnP1wtHzgNlJSvkbzB-7dYHENBGxHnxACcnsu8sr8130_provenance.
- NP304113.RAF7uGzquW7qLHwpF1-4X8G-peI8BguQ6gOdD1s1RPy6w130_assertion description "[Our findings document that patients carrying these SCAD gene variations may develop clinically relevant SCAD deficiency, and that patients with even mild ethylmalonic aciduria should be tested for these variations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP304113.RAF7uGzquW7qLHwpF1-4X8G-peI8BguQ6gOdD1s1RPy6w130_provenance.