A missense mutation in Grm6 reduces but does not eliminate mGluR6 expression or rod depolarizing bipolar cell function
2017 ◽
Vol 118
(2)
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pp. 845-854
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Keyword(s):
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.
2012 ◽
Vol 90
(2)
◽
pp. 331-339
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2009 ◽
Vol 85
(5)
◽
pp. 711-719
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Keyword(s):
Keyword(s):
Keyword(s):