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- W2613443709 abstract "This article describes a mouse model of the human disease complete congenital stationary night blindness in which the mutation reduces but does not eliminate GRM6 expression and bipolar cell function, a phenotype distinct from that seen in other Grm6 mouse models." @default.
- W2613443709 created "2017-05-19" @default.
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- W2613443709 date "2017-08-01" @default.
- W2613443709 modified "2023-10-14" @default.
- W2613443709 title "A missense mutation in <i>Grm6</i> reduces but does not eliminate mGluR6 expression or rod depolarizing bipolar cell function" @default.
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- W2613443709 doi "https://doi.org/10.1152/jn.00888.2016" @default.
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