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Q24313099-B70B3A05-F24E-4FE0-AF49-E8643F779E69
Q24313099-B70B3A05-F24E-4FE0-AF49-E8643F779E69
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http://www.wikidata.org/entity/statement/Q24313099-B70B3A05-F24E-4FE0-AF49-E8643F779E69
Recessive mutations of the gene TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humans
P2860
Q24313099-B70B3A05-F24E-4FE0-AF49-E8643F779E69
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24313099-B70B3A05-F24E-4FE0-AF49-E8643F779E69
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wasDerivedFrom
d8b96d459d0ee148296caadd0b0b4f943170511d
P2860
Chromosomal localization and genomic characterization of the mouse melastatin gene (Mlsn1)