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
Publicado en:J Korean Med Sci
Main Authors: Kim, Min Seok, Joo, Kwangsic, Seong, Moon-Woo, Kim, Man Jin, Park, Kyu Hyung, Park, Sung Sup, Woo, Se Joon
Formato: Artigo
Idioma:Inglês
Publicado: The Korean Academy of Medical Sciences 2019
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Original Article
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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