Genetic analysis of chromosome 20-related posterior polymorphous corneal dystrophy: genetic heterogeneity and exclusion of three candidate genes

PURPOSE: Posterior polymorphous corneal dystrophy (PPCD) is a genetically heterogeneous autosomal dominant condition which maps to the pericentromeric region of chromosome 20. Mutations in the VSX1 transcription factor have been reported in patients affected with PPCD, keratoconus, or a combination...

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Detalles Bibliográficos
Autores principales: Hosseini, S. Mohsen, Herd, Sarah, Vincent, Andrea L., Héon, Elise
Formato: Texto
Lenguaje:English
Publicado: Molecular Vision 2008
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2267740/
https://www.ncbi.nlm.nih.gov/pubmed/18253095

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2267740/
https://www.ncbi.nlm.nih.gov/pubmed/18253095

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