Molecular characterization of Leber congenital amaurosis in Koreans

PURPOSE: Leber congenital amaurosis (LCA) is the most severe form of inherited retinal dystrophy, and invariably leads to blindness. LCA is a genetically and clinically heterogenous disorder. Although more than nine genes have been found to be associated with LCA, they only account for about half of...

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Detalles Bibliográficos
Autores principales: Seong, Moon-Woo, Kim, Seong Yeon, Yu, Young Suk, Hwang, Jeong-Min, Kim, Ji Yeon, Park, Sung Sup
Formato: Texto
Lenguaje:English
Publicado: Molecular Vision 2008
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2493025/
https://www.ncbi.nlm.nih.gov/pubmed/18682808

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2493025/
https://www.ncbi.nlm.nih.gov/pubmed/18682808

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