T-cell infiltration in autosomal dominant neovascular inflammatory vitreoretinopathy.
Vinit B. Mahajan(Stanford University), Edwin M. Stone(Instituto da Visão)
PubMed
June 8, 2010
Cited by 15
Related Papers
Age-dependent effects of RPE65 gene therapy for Leber's congenital amaurosis: a phase 1 dose-escalation trial
|The Lancet|2009|857
Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate
|Nature Genetics|2000|506
Mutations in MKKS cause Bardet-Biedl syndrome
|Nature Genetics|2000|270
Three autosomal dominant corneal dystrophies map to chromosome 5q
|Nature Genetics|1994|170
Avellino Corneal Dystrophy
|Ophthalmology|1992|143