Matches in Nanopublications for { ?s ?p "[Mutations in IMPDH1 account for approximately 2% of families with adRP, and de novo IMPDH1 mutations are also rare causes of isolated LCA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP20192.RAZ-X3Af4IL174x6VHZySDsdPacKAzL04NLaVe1tDFSeE130_assertion description "[Mutations in IMPDH1 account for approximately 2% of families with adRP, and de novo IMPDH1 mutations are also rare causes of isolated LCA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP20192.RAZ-X3Af4IL174x6VHZySDsdPacKAzL04NLaVe1tDFSeE130_provenance.
- NP20194.RAbIUti1d4-f4An9RZ_2sDCeJqqsdYp8VxW4F5J2XFBaU130_assertion description "[Mutations in IMPDH1 account for approximately 2% of families with adRP, and de novo IMPDH1 mutations are also rare causes of isolated LCA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP20194.RAbIUti1d4-f4An9RZ_2sDCeJqqsdYp8VxW4F5J2XFBaU130_provenance.
- assertion description "[Mutations in IMPDH1 account for approximately 2% of families with adRP, and de novo IMPDH1 mutations are also rare causes of isolated LCA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.