Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus | Nature Genetics
Coats Plus Syndrome and Mutation of the TERT Gene: A Case Report
Cerebro-retinal microangiopathy with calcifications and cysts due to recessive mutations in the CTC1 gene. | Semantic Scholar
Teaching NeuroImages: Adult-onset leukoencephalopathy with intracranial calcifications and cysts (Labrune syndrome) | Neurology
Coats Plus Syndrome.,JAMA Neurology - X-MOL
Coats plus syndrome: MedlinePlus Genetics
PDF) Retinopathy and bone marrow failure revealing Coats plus syndrome
Coats plus syndrome: MedlinePlus Genetics
Coats plus syndrome: a rare cause of severe gastrointestinal tract bleeding in children – a case report | BMC Pediatrics | Full Text
Coats plus syndrome (cerebroretinal microangiopathy with calcifications and cysts‐1): A case report - Morgado - 2021 - Pediatric Dermatology - Wiley Online Library
Brain Sciences | Free Full-Text | Leukoencephalopathy with Calcifications and Cysts—The First Polish Patient with Labrune Syndrome
Coats Plus : la version systémique de la maladie de Coats | Semantic Scholar
Coats plus syndrome with new observation of drusenoid retinal pigment epithelial detachments in a teenager - ScienceDirect
Coats Disease and Coats Plus Syndrome - ScienceDirect
Coats plus syndrome: MedlinePlus Genetics
Cerebroretinal microangiopathy with calcifications and cysts - Wikipedia