Matches in Nanopublications for { ?s ?p "[The demonstration that mutations in a gene previously associated with recessive Leber congenital amaurosis can also cause dominant RP illustrates the wide phenotypic variability of retinal degeneration genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP122344.RAgQBmrQfJHmZUk-RUG-ALwPaWH5QMhrXyp5x6RZXRP00130_assertion description "[The demonstration that mutations in a gene previously associated with recessive Leber congenital amaurosis can also cause dominant RP illustrates the wide phenotypic variability of retinal degeneration genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP122344.RAgQBmrQfJHmZUk-RUG-ALwPaWH5QMhrXyp5x6RZXRP00130_provenance.
- assertion description "[The demonstration that mutations in a gene previously associated with recessive Leber congenital amaurosis can also cause dominant RP illustrates the wide phenotypic variability of retinal degeneration genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP241795.RAvS1-SP3d3BgQLs1UCBxMa91HINOX6FzAsyuTxhJ4Y0M130_assertion description "[The demonstration that mutations in a gene previously associated with recessive Leber congenital amaurosis can also cause dominant RP illustrates the wide phenotypic variability of retinal degeneration genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP241795.RAvS1-SP3d3BgQLs1UCBxMa91HINOX6FzAsyuTxhJ4Y0M130_provenance.
- NP185531.RA3FNmGFPZ25ZFV8ry3QczuDExajzNT2mY7dZhCy7mB_8130_assertion description "[The demonstration that mutations in a gene previously associated with recessive Leber congenital amaurosis can also cause dominant RP illustrates the wide phenotypic variability of retinal degeneration genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185531.RA3FNmGFPZ25ZFV8ry3QczuDExajzNT2mY7dZhCy7mB_8130_provenance.