Cargando...
KCNV2 retinopathy: clinical features, molecular genetics and directions for future therapy
ABSTRACT. -associated retinopathy or “cone dystrophy with supernormal rod responses” is an autosomal recessive cone-rod dystrophy with pathognomonic ERG findings. This gene encodes Kv8.2, a voltage-gated potassium channel subunit that acts as a modulator by shifting the activation range of the K(+)...
Gardado en:
| Publicado en: | Ophthalmic Genet |
|---|---|
| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Taylor & Francis
2020
|
| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7446039/ https://ncbi.nlm.nih.gov/pubmed/32441199 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/13816810.2020.1766087 |
| Tags: |
Engadir etiqueta
Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!
|