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Electroretinographic findings in a patient with congenital stationary night blindness due to a novel NYX mutation
PURPOSE: To document a novel NYX gene mutation in a patient with X-linked complete congenital stationary night blindness and to describe this patient’s electroretinogram (ERG) characteristics. METHODS: ERGs were recorded from a 17-year-old male with a previously unreported NYX mutation (819G>A) t...
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| Autors principals: | , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2013
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3842226/ https://ncbi.nlm.nih.gov/pubmed/23289809 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3109/13816810.2012.743570 |
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