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Depolarizing bipolar cell dysfunction due to a Trpm1 point mutation
Mutations in TRPM1 are found in humans with an autosomal recessive form of complete congenital stationary night blindness (cCSNB). The Trpm1(−/−) mouse has been an important animal model for this condition. Here we report a new mouse mutant, tvrm27, identified in a chemical mutagenesis screen. Genet...
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| Hlavní autoři: | , , , , , , , , , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
American Physiological Society
2012
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3545183/ https://ncbi.nlm.nih.gov/pubmed/22896717 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/jn.00137.2012 |
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