Matches in Nanopublications for { ?s ?p "[To clinically characterize a Swedish family with autosomal dominant retinitis pigmentosa due to a mutation, Arg-172-Trp, in the peripherin/RDS gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP1407866.RAqdzFKWjSsmCQ9rkgnJvCqNa0Frkj_K3BDhaG4_BZvJw130_assertion description "[To clinically characterize a Swedish family with autosomal dominant retinitis pigmentosa due to a mutation, Arg-172-Trp, in the peripherin/RDS gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1407866.RAqdzFKWjSsmCQ9rkgnJvCqNa0Frkj_K3BDhaG4_BZvJw130_provenance.
- NP668589.RAFZEk7oaiZRLxOK3dgtmKfo30hmtE225FsAqfPfzuG9I130_assertion description "[To clinically characterize a Swedish family with autosomal dominant retinitis pigmentosa due to a mutation, Arg-172-Trp, in the peripherin/RDS gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668589.RAFZEk7oaiZRLxOK3dgtmKfo30hmtE225FsAqfPfzuG9I130_provenance.