Careful clinical-functional phenotyping combined with systematic, broad NGS Panel-based genotyping identify numerous novel disease-causing mutations and deletions in inherited retinal dystrophy (IRD) patients
- Resource Type
- Journal
- Authors
- Iannaccone, Alessandro; Berdia, Jay; Kheir, Wajiha; Mighion, Lindsay; Wang, Nicholas; DaSilva, Cristina; Duan, Jie; Alexander, John J.; Chiang, John (P-W)
- Source
- INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE; JUL 2018, 59 9, 3p.
- Subject
- Language
- English
- ISSN
- 15525783