Novel compound heterozygous STN1 variants are associated with Coats Plus syndrome - Acharya - 2021 - Molecular Genetics & Genomic Medicine - Wiley Online Library
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
Retinopathy and bone marrow failure revealing Coats plus syndrome | BMJ Case Reports
Coats Plus Syndrome | Hereditary Ocular Diseases
Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus | Nature Genetics
PDF] Mutations in STN1 cause Coats plus syndrome and are associated with genomic and telomere defects | Semantic Scholar