A Novel Form of Transducin-Dependent Retinal Degeneration: Accelerated Retinal Degeneration in the Absence of Rod Transducin

PURPOSE: Rhodopsin mutations account for approximately 25% of human autosomal dominant retinal degenerations. However, the molecular mechanisms by which rhodopsin mutations cause photoreceptor cell death are unclear. Mutations in genes involved in the termination of rhodopsin signaling activity have...

Ful tanımlama

Kaydedildi:
Detaylı Bibliyografya
Asıl Yazarlar: Brill, Elliott, Malanson, Katherine M., Radu, Roxana A., Boukharov, Natalia V., Wang, Zhongyan, Chung, Hae-Yun, Lloyd, Marcia B., Bok, Dean, Travis, Gabriel H., Obin, Martin, Lem, Janis
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2007
Konular:
Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC2248236/
https://ncbi.nlm.nih.gov/pubmed/18055791
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1167/iovs.06-1402
Etiketler: Etiketle
Etiket eklenmemiş, İlk siz ekleyin!

Benzer Materyaller