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PDFLaboratory science
C21orf2 is mutated in recessive early-onset retinal dystrophy with macular staphyloma and encodes a protein that localises to the photoreceptor primary cilium
- Correspondence to Dr Arif O Khan, Division of Pediatric Ophthalmology, King Khaled Eye Specialist Hospital, PO Box 7191, Riyadh 11462, Saudi Arabia; arif.khan{at}mssm.edu
Citation
C21orf2 is mutated in recessive early-onset retinal dystrophy with macular staphyloma and encodes a protein that localises to the photoreceptor primary cilium
Publication history
- Received June 8, 2015
- Revised July 22, 2015
- Accepted August 1, 2015
- First published August 20, 2015.
Online issue publication
November 20, 2015
Article Versions
- Previous version (20 August 2015).
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