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 (Leber congenital amaurosis).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP122354.RAzbc4FcvUet2xe48c3HI0T71Xd8J37moatpIZGwG5a5Y130_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 (Leber congenital amaurosis).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP122354.RAzbc4FcvUet2xe48c3HI0T71Xd8J37moatpIZGwG5a5Y130_provenance.
- NP185541.RAd3qjydWwzNZBlTS8LuT4fpOhoHpY276SaSrhU19cDwI130_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 (Leber congenital amaurosis).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185541.RAd3qjydWwzNZBlTS8LuT4fpOhoHpY276SaSrhU19cDwI130_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 (Leber congenital amaurosis).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP214833.RAPyEn5fNwockUryCt0S1CO-iebAAU9bxtbmbQvhHaNhk130_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 (Leber congenital amaurosis).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP214833.RAPyEn5fNwockUryCt0S1CO-iebAAU9bxtbmbQvhHaNhk130_provenance.