Matches in Nanopublications for { ?s ?p "[Large deletions of the KCNV2 gene are common in patients with cone dystrophy with supernormal rod response.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP390886.RAMMKq2T2kvvXSfsgOP_WbVHhEQXLIYvgojeJ77eOBrnE130_assertion description "[Large deletions of the KCNV2 gene are common in patients with cone dystrophy with supernormal rod response.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390886.RAMMKq2T2kvvXSfsgOP_WbVHhEQXLIYvgojeJ77eOBrnE130_provenance.
- assertion description "[Large deletions of the KCNV2 gene are common in patients with cone dystrophy with supernormal rod response.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP978023.RAtI_N7b4X3yNX_Kn97kN2NHP4C3le64Cqu5ppOlas3do130_assertion description "[Large deletions of the KCNV2 gene are common in patients with cone dystrophy with supernormal rod response.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978023.RAtI_N7b4X3yNX_Kn97kN2NHP4C3le64Cqu5ppOlas3do130_provenance.
- NP920669.RA2Co4EhmYpEHQE09LwJ0JfIzji0uWerogChS7mJouZpM130_assertion description "[Large deletions of the KCNV2 gene are common in patients with cone dystrophy with supernormal rod response.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP920669.RA2Co4EhmYpEHQE09LwJ0JfIzji0uWerogChS7mJouZpM130_provenance.