Matches in Nanopublications for { ?s ?p "[Incomplete X-linked congenital stationary night blindness (CSNB) is a clinically variable condition that has been shown to be caused by mutations in the calcium-channel CACNA1F gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 1 of
1
with 100 items per page.
- NP563811.RAKuHdqJKNvZLR2G5N8PUkGdT1YTM5dPry1A9TGnwMbIo130_assertion description "[Incomplete X-linked congenital stationary night blindness (CSNB) is a clinically variable condition that has been shown to be caused by mutations in the calcium-channel CACNA1F gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP563811.RAKuHdqJKNvZLR2G5N8PUkGdT1YTM5dPry1A9TGnwMbIo130_provenance.