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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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Detalles Bibliográficos
Autores principales:	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:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2019
Materias:	Original Paper
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6826137/ https://www.ncbi.nlm.nih.gov/pubmed/31385385 http://dx.doi.org/10.1111/acel.13011

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