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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Bibliografiske detaljer
Udgivet i: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
Format: Artigo
Sprog:Inglês
Udgivet: John Wiley and Sons Inc. 2019
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Original Paper
Online adgang: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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