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Genetic Mutation Profiles in Korean Patients with Inherited Retinal Diseases
BACKGROUND: Because of genetically and phenotypically heterogenous features, identification of causative genes for inherited retinal diseases (IRD) is essential for diagnosis and treatment in coming gene therapy era. To date, there are no large-scale data of the genes responsible for IRD in Korea. T...
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| Publicado en: | J Korean Med Sci |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
The Korean Academy of Medical Sciences
2019
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6543061/ https://ncbi.nlm.nih.gov/pubmed/31144483 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3346/jkms.2019.34.e161 |
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