The Role of the Voltage-Gated Potassium Channel Proteins Kv8.2 and Kv2.1 in Vision and Retinal Disease: Insights from the Study of Mouse Gene Knock-Out Mutations

Mutations in the KCNV2 gene, which encodes the voltage-gated K(+) channel protein Kv8.2, cause a distinctive form of cone dystrophy with a supernormal rod response (CDSRR). Kv8.2 channel subunits only form functional channels when combined in a heterotetramer with Kv2.1 subunits encoded by the KCNB1...

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Detalles Bibliográficos
Autores principales: Hart, Nathan S., Mountford, Jessica K., Voigt, Valentina, Fuller-Carter, Paula, Barth, Melanie, Nerbonne, Jeanne M., Hunt, David M., Carvalho, Livia S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Neuroscience 2019
Materias:
New Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6393689/
https://www.ncbi.nlm.nih.gov/pubmed/30820446
http://dx.doi.org/10.1523/ENEURO.0032-19.2019

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6393689/
https://www.ncbi.nlm.nih.gov/pubmed/30820446
http://dx.doi.org/10.1523/ENEURO.0032-19.2019

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