Novel RCBTB1 variants causing later-onset non-syndromic retinal dystrophy with macular chorioretinal atrophy
- Resource Type
- Source
- Ophthalmic Genetics. 43:332-339
- Subject
Ophthalmology Pediatrics, Perinatology and Child Health Genetics (clinical) - Language
- ISSN
- 1744-5094
1381-6810