Researchers identify a new genetic cause of C | EurekAlert!
Cerebro-retinal microangiopathy with calcifications and cysts due to recessive mutations in the CTC1 gene - ScienceDirect
Coats plus syndrome: MedlinePlus Genetics
Coats plus syndrome: MedlinePlus Genetics
Coats Disease | Ento Key
Teaching NeuroImages: Adult-onset leukoencephalopathy with intracranial calcifications and cysts (Labrune syndrome) | Neurology
Coats Disease: Treatment, Stages, and Symptoms
Coats' disease - Wikipedia
Novel compound heterozygous STN1 variants are associated with Coats Plus syndrome - Acharya - 2021 - Molecular Genetics & Genomic Medicine - Wiley Online Library
Coats Plus Syndrome and Mutation of the TERT Gene: A Case Report
Diagnosis and treatment of bilateral Coats disease in a 5-year-old girl - Journal of American Association for Pediatric Ophthalmology and Strabismus {JAAPOS}
Coats Plus Syndrome.,JAMA Neurology - X-MOL
Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus | Nature Genetics
Coats plus syndrome: a rare cause of severe gastrointestinal tract bleeding in children – a case report | BMC Pediatrics | Full Text
Coats plus syndrome: MedlinePlus Genetics
Coats Plus : la version systémique de la maladie de Coats | Semantic Scholar
Efficacy of Systemic Bevacizumab on Coats Plus Syndrome - Ophthalmology Retina
Coats plus syndrome (cerebroretinal microangiopathy with calcifications and cysts‐1): A case report - Morgado - 2021 - Pediatric Dermatology - Wiley Online Library
Coats Plus : la version systémique de la maladie de Coats | Semantic Scholar
Coats plus syndrome phenotype and mutation analysis of the CTC1 and... | Download Scientific Diagram
Retinopathy and bone marrow failure revealing Coats plus syndrome | BMJ Case Reports
Coats plus syndrome: MedlinePlus Genetics
