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Coats plus syndrome (cerebroretinal microangiopathy with calcifications and cysts‐1): A case report - Morgado - 2021 - Pediatric Dermatology - Wiley Online Library
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Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus | Nature Genetics
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PDF] Mutations in STN1 cause Coats plus syndrome and are associated with genomic and telomere defects | Semantic Scholar
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Cerebro-retinal microangiopathy with calcifications and cysts due to recessive mutations in the CTC1 gene - ScienceDirect
![Teaching NeuroImages: Adult-onset leukoencephalopathy with intracranial calcifications and cysts (Labrune syndrome) | Neurology Teaching NeuroImages: Adult-onset leukoencephalopathy with intracranial calcifications and cysts (Labrune syndrome) | Neurology](https://n.neurology.org/content/neurology/88/12/e113/F1.large.jpg)
Teaching NeuroImages: Adult-onset leukoencephalopathy with intracranial calcifications and cysts (Labrune syndrome) | Neurology
![PDF) Retinopathy and bone marrow failure revealing Coats plus syndrome | Paula Kjöllerström - Academia.edu PDF) Retinopathy and bone marrow failure revealing Coats plus syndrome | Paula Kjöllerström - Academia.edu](https://0.academia-photos.com/attachment_thumbnails/73665654/mini_magick20211026-25666-1ahrl6n.png?1635258398)
PDF) Retinopathy and bone marrow failure revealing Coats plus syndrome | Paula Kjöllerström - Academia.edu
![Stage 4 Coats disease showing bullous exudative retinal detachment and... | Download Scientific Diagram Stage 4 Coats disease showing bullous exudative retinal detachment and... | Download Scientific Diagram](https://www.researchgate.net/publication/333484917/figure/fig1/AS:764244492578817@1559221494245/Stage-4-Coats-disease-showing-bullous-exudative-retinal-detachment-and-irregular.png)