A Case of Korean Patient with Macular Corneal Dystrophy Associated with Novel Mutation in the CHST6 Gene

To report a novel mutation within the CHST6 gene, as well as describe light and electron microscopic features of a case of macular corneal dystrophy. A 59-year old woman with macular corneal dystrophy in both eyes who had decreased visual acuity underwent penetrating keratoplasty. Further studies in...

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Detalles Bibliográficos
Autores principales: Lee, You Kyung, Chang, Dong-Jin, Chung, Sung Kun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Ophthalmological Society 2013
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3849310/
https://www.ncbi.nlm.nih.gov/pubmed/24311932
http://dx.doi.org/10.3341/kjo.2013.27.6.454

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3849310/
https://www.ncbi.nlm.nih.gov/pubmed/24311932
http://dx.doi.org/10.3341/kjo.2013.27.6.454

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