Molecular, Cellular and Functional Changes in the Retinas of Young Adult Mice Lacking the Voltage-Gated K(+) Channel Subunits Kv8.2 and K2.1

Cone Dystrophy with Supernormal Rod Response (CDSRR) is a rare autosomal recessive disorder leading to severe visual impairment in humans, but little is known about its unique pathophysiology. We have previously shown that CDSRR is caused by mutations in the KCNV2 (Potassium Voltage-Gated Channel Mo...

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Detalles Bibliográficos
Autores principales: Jiang, Xiaotian, Rashwan, Rabab, Voigt, Valentina, Nerbonne, Jeanne, Hunt, David M., Carvalho, Livia S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8124447/
https://www.ncbi.nlm.nih.gov/pubmed/34063002
http://dx.doi.org/10.3390/ijms22094877

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8124447/
https://www.ncbi.nlm.nih.gov/pubmed/34063002
http://dx.doi.org/10.3390/ijms22094877

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