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Q30490821-A111B15D-8077-4C88-9F91-9C184ADD6E47
Q30490821-A111B15D-8077-4C88-9F91-9C184ADD6E47
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http://www.wikidata.org/entity/statement/Q30490821-A111B15D-8077-4C88-9F91-9C184ADD6E47
REPEATABILITY AND LONGITUDINAL ASSESSMENT OF FOVEAL CONE STRUCTURE IN CNGB3-ASSOCIATED ACHROMATOPSIA.
P2860
Q30490821-A111B15D-8077-4C88-9F91-9C184ADD6E47
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30490821-A111B15D-8077-4C88-9F91-9C184ADD6E47
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wasDerivedFrom
5ef31879fbd4c9ff260df85b2308f6cbca06ca8a
P2860
Total colourblindness is caused by mutations in the gene encoding the alpha-subunit of the cone photoreceptor cGMP-gated cation channel