Yüklüyor......

Normal GCAPs partly compensate for altered cGMP signaling in retinal dystrophies associated with mutations in GUCA1A

Missense mutations in the GUCA1A gene encoding guanylate cyclase-activating protein 1 (GCAP1) are associated with autosomal dominant cone/cone-rod (CORD) dystrophies. The nature of the inheritance pattern implies that a pool of normal GCAP proteins is present in photoreceptors together with the muta...

Ful tanımlama

Kaydedildi:
Detaylı Bibliyografya
Yayımlandı:Sci Rep
Asıl Yazarlar: Dell’Orco, Daniele, Dal Cortivo, Giuditta
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Nature Publishing Group UK 2019
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC6934868/
https://ncbi.nlm.nih.gov/pubmed/31882816
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-019-56606-5
Etiketler: Etiketle
Etiket eklenmemiş, İlk siz ekleyin!