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Survey of the nob5 mutation in C3H substrains
PURPOSE: A no b-wave (nob) electroretinography (ERG) phenotype arose spontaneously in a colony of C3H mice and was named nob5. A mutation was identified in the Gpr179 gene in homozygous nob5 mice. There is a concern that this mutation is also present in additional C3H sublines and may compromise ret...
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Molecular Vision
2015
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4575902/ https://www.ncbi.nlm.nih.gov/pubmed/26396487 |