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Q51062868-1538E5AD-38C5-4852-9E56-1161B9DD1B40
Q51062868-1538E5AD-38C5-4852-9E56-1161B9DD1B40
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51062868-1538E5AD-38C5-4852-9E56-1161B9DD1B40
Congenital Achromatopsia and Macular Atrophy Caused by a Novel Recessive PDE6C Mutation (p.E591K).
P2860
Q51062868-1538E5AD-38C5-4852-9E56-1161B9DD1B40
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51062868-1538E5AD-38C5-4852-9E56-1161B9DD1B40
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wasDerivedFrom
91a2c0cec7abca65e081cf4d903fac1b443900bf
P2860
Total colourblindness is caused by mutations in the gene encoding the alpha-subunit of the cone photoreceptor cGMP-gated cation channel