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Congenital Stationary Night Blindness due to Novel TRPM1 Gene Mutations in a Korean Patient
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| Publicat a: | Korean J Ophthalmol |
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| Autors principals: | , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
The Korean Ophthalmological Society
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7105792/ https://ncbi.nlm.nih.gov/pubmed/32233153 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3341/kjo.2019.0080 |
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