Screening the visual system homeobox 1 gene in keratoconus and posterior polymorphous dystrophy cohorts identifies a novel variant

PURPOSE: Mutations in the visual system homeobox 1 (VSX1) gene have been described at a low frequency in keratoconus and posterior polymorphous corneal dystrophy (PPCD). The putative role is controversial for several reasons, including a lack of mutations detected in other population cohorts. This s...

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Detalles Bibliográficos
Autores principales: Vincent, Andrea L., Jordan, Charlotte, Sheck, Leo, Niederer, Rachel, Patel, Dipika V., McGhee, Charles N.J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3626301/
https://www.ncbi.nlm.nih.gov/pubmed/23592923

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