Late‐onset retinal degeneration pathology due to mutations in CTRP5 is mediated through HTRA1

Late‐onset retinal degeneration (L‐ORD) is an autosomal dominant macular degeneration characterized by the formation of sub‐retinal pigment epithelium (RPE) deposits and neuroretinal atrophy. L‐ORD results from mutations in the C1q‐tumor necrosis factor‐5 protein (CTRP5), encoded by the CTRP5/C1QTNF...

Cijeli opis

Spremljeno u:
Bibliografski detalji
Izdano u:Aging Cell
Glavni autori: Chekuri, Anil, Zientara‐Rytter, Katarzyna, Soto‐Hermida, Angel, Borooah, Shyamanga, Voronchikhina, Marina, Biswas, Pooja, Kumar, Virender, Goodsell, David, Hayward, Caroline, Shaw, Peter, Stanton, Chloe, Garland, Donita, Subramani, Suresh, Ayyagari, Radha
Format: Artigo
Jezik:Inglês
Izdano: John Wiley and Sons Inc. 2019
Teme:
Original Paper
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6826137/
https://ncbi.nlm.nih.gov/pubmed/31385385
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/acel.13011
Oznake: Dodaj oznaku
Bez oznaka, Budi prvi tko označuje ovaj zapis!

Similar Items