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Identification of a new mutant allele, Grm6(nob7), for complete congenital stationary night blindness
Electroretinogram (ERG) studies identified a new mouse line with a normal a-wave but lacking the b-wave component. The ERG phenotype of this new allele, nob7, matched closely that of mouse mutants for Grm6, Lrit3, Trpm1, and Nyx, which encode for proteins expressed in depolarizing bipolar cells (DBC...
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| Vydáno v: | Vis Neurosci |
|---|---|
| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2015
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4648616/ https://ncbi.nlm.nih.gov/pubmed/26241901 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1017/S0952523815000012 |
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