Matches in Nanopublications for { ?s ?p "[These findings strongly implicate defects of RDH5 as the cause of fundus albipunctatus and point to a heterogeneity of RDH5 mutations in this form of congenital stationary night blindness with variable expressivity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP329243.RARUoJdQZmGxkvSo7FjmPsVGTf-xNWSrjXSp5cVj2slA8130_assertion description "[These findings strongly implicate defects of RDH5 as the cause of fundus albipunctatus and point to a heterogeneity of RDH5 mutations in this form of congenital stationary night blindness with variable expressivity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP329243.RARUoJdQZmGxkvSo7FjmPsVGTf-xNWSrjXSp5cVj2slA8130_provenance.
- NP5474.RAPdHZ9Cm5loo6sj-YQXi7ifmV2c7BtiHAfbGJh3pfLT4130_assertion description "[These findings strongly implicate defects of RDH5 as the cause of fundus albipunctatus and point to a heterogeneity of RDH5 mutations in this form of congenital stationary night blindness with variable expressivity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP5474.RAPdHZ9Cm5loo6sj-YQXi7ifmV2c7BtiHAfbGJh3pfLT4130_provenance.