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...

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Detalhes bibliográficos
Publicado no:Aging Cell
Main Authors: 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
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2019
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Original Paper
Acesso em linha: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
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