Matches in Nanopublications for { ?s ?p "[To report novel spectral domain optical coherence tomography (SD-OCT) findings and new mutational data in patients with 'cone dystrophy with supernormal rod electroretinogram', a recessive childhood onset retinal dystrophy consequent upon mutation in the KCNV2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP978029.RAark1buBisaVdGZKopv1F9qXmnSn-_elTPpZ3UOXvpWc130_assertion description "[To report novel spectral domain optical coherence tomography (SD-OCT) findings and new mutational data in patients with 'cone dystrophy with supernormal rod electroretinogram', a recessive childhood onset retinal dystrophy consequent upon mutation in the KCNV2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978029.RAark1buBisaVdGZKopv1F9qXmnSn-_elTPpZ3UOXvpWc130_provenance.
- NP892995.RAMlrYXVmZCbIdZMn5gG2nA-Z92BZRPKwP9IckSIL6CTQ130_assertion description "[To report novel spectral domain optical coherence tomography (SD-OCT) findings and new mutational data in patients with 'cone dystrophy with supernormal rod electroretinogram', a recessive childhood onset retinal dystrophy consequent upon mutation in the KCNV2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP892995.RAMlrYXVmZCbIdZMn5gG2nA-Z92BZRPKwP9IckSIL6CTQ130_provenance.