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Q38793661-FDF9D027-298B-4DEE-A356-CB93EA4B7925
Q38793661-FDF9D027-298B-4DEE-A356-CB93EA4B7925
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38793661-FDF9D027-298B-4DEE-A356-CB93EA4B7925
A missense mutation in Grm6 reduces but does not eliminate mGluR6 expression or rod depolarizing bipolar cell function.
P2860
Q38793661-FDF9D027-298B-4DEE-A356-CB93EA4B7925
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38793661-FDF9D027-298B-4DEE-A356-CB93EA4B7925
rank
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wasDerivedFrom
ecbfd1280c4dfee7d2e75c489fec3dd9ce6a0457
P2860
Mutations in GRM6 cause autosomal recessive congenital stationary night blindness with a distinctive scotopic 15-Hz flicker electroretinogram.