Ophthalmic findings and a novel CTC1 gene mutation in coats plus syndrome: a case report.

CONCLUSIONS: The present report expanded the genotype and phenotype spectrum of CTC1 gene associated with Coats plus syndrome. PMID: 33034244 [PubMed - as supplied by publisher]
Source: Ophthalmic Genetics - Category: Opthalmology Tags: Ophthalmic Genet Source Type: research