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Q36257781-35EC4FFA-6A17-4299-9A13-B1748AF9CFB5
Q36257781-35EC4FFA-6A17-4299-9A13-B1748AF9CFB5
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http://www.wikidata.org/entity/statement/Q36257781-35EC4FFA-6A17-4299-9A13-B1748AF9CFB5
Mutations in GRM6 identified in consanguineous Pakistani families with congenital stationary night blindness.
P2860
Q36257781-35EC4FFA-6A17-4299-9A13-B1748AF9CFB5
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36257781-35EC4FFA-6A17-4299-9A13-B1748AF9CFB5
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wasDerivedFrom
488531a302da11da9ec182931d62d3fb59d0715b
P2860
Mutations in TRPM1 are a common cause of complete congenital stationary night blindness