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Q35011677-A60B9A28-B7BF-4AEF-8A9E-38564966C2CB
Q35011677-A60B9A28-B7BF-4AEF-8A9E-38564966C2CB
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Statement
http://www.wikidata.org/entity/statement/Q35011677-A60B9A28-B7BF-4AEF-8A9E-38564966C2CB
TRPM1 is mutated in patients with autosomal-recessive complete congenital stationary night blindness.
P2860
Q35011677-A60B9A28-B7BF-4AEF-8A9E-38564966C2CB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35011677-A60B9A28-B7BF-4AEF-8A9E-38564966C2CB
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wasDerivedFrom
c973f5e87fd9f244ac3032fcef9b513d79f0fbc7
P2860
Mutations in GRM6 cause autosomal recessive congenital stationary night blindness with a distinctive scotopic 15-Hz flicker electroretinogram.