Night blindness–associated mutations in
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Christina Zeitz; Ursula Forster; John Neidhardt; Silke Feil; Stefan Kälin; Dorot
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Article
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2007
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John Wiley and Sons
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English
⚖ 454 KB
Mutations in the GRM6 gene, which encodes the metabotropic glutamate receptor 6 (mGluR6), lead to autosomal recessive congenital stationary night blindness (CSNB), which is characterized by loss of night vision due to a defect in signal transmission from photoreceptor to the adjacent ON-bipolar cell