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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Detalles Bibliográficos
Autores principales: Kim, Min Seok, Joo, Kwangsic, Seong, Moon-Woo, Kim, Man Jin, Park, Kyu Hyung, Park, Sung Sup, Woo, Se Joon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Academy of Medical Sciences 2019
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6543061/
https://www.ncbi.nlm.nih.gov/pubmed/31144483
http://dx.doi.org/10.3346/jkms.2019.34.e161

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6543061/
https://www.ncbi.nlm.nih.gov/pubmed/31144483
http://dx.doi.org/10.3346/jkms.2019.34.e161

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