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The Expression of Whirlin and Ca(v)1.3α(1) is Mutually Independent in Photoreceptors
Whirlin is a gene responsible for Usher syndrome type II (USH2) and congenital deafness. In photoreceptors, it organizes a protein complex through binding to proteins encoded by other USH2 genes, usherin (USH2A) and G-protein-coupled receptor 98 (GPR98). Recently, Ca(v)1.3α(1) (α(1D)) has been disco...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3514573/ https://ncbi.nlm.nih.gov/pubmed/22892111 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.visres.2012.07.020 |
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