Matches in Nanopublications for { ?s ?p "[To describe in detail the characteristic clinical phenotype and electrophysiological features of Severe Early Childhood Onset Retinal Dystrophy (SECORD) caused by mutation of RPE65.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP445198.RAWKBfI35WgjaPi1zCcdyYw6Bi1cQ9nUVkM1wcQz3agyE130_assertion description "[To describe in detail the characteristic clinical phenotype and electrophysiological features of Severe Early Childhood Onset Retinal Dystrophy (SECORD) caused by mutation of RPE65.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP445198.RAWKBfI35WgjaPi1zCcdyYw6Bi1cQ9nUVkM1wcQz3agyE130_provenance.