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GNAT1 Associated with Autosomal Recessive Congenital Stationary Night Blindness
PURPOSE. Congenital stationary night blindness is a nonprogressive retinal disorder manifesting as impaired night vision and is generally associated with other ocular symptoms, such as nystagmus, myopia, and strabismus. This study was conducted to further investigate the genetic basis of CSNB in a c...
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| Autori principali: | , , , , , , , , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Association for Research in Vision and Ophthalmology, Inc.
2012
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3339909/ https://ncbi.nlm.nih.gov/pubmed/22190596 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1167/iovs.11-8026 |
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