Exclusion of Positional Candidate Gene Coding Region Mutations in the Common Posterior Polymorphous Corneal Dystrophy 1 Candidate Gene Interval

PURPOSE: Posterior polymorphous corneal dystrophy (PPCD) is an autosomal dominant disorder of the corneal endothelium associated with visually significant corneal edema and glaucoma. Statistical genetic analysis of four families with PPCD has demonstrated linkage to a 2.4 cM common support interval...

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Main Authors: Aldave, Anthony J., Yellore, Vivek S., Vo, Rosalind C., Kamal, Khairidzan M., Rayner, Sylvia A., Plaisier, Christopher L, Chen, Michael C., Damani, Mausam R., Pham, Michele N., Gorin, Michael B., Sobel, Eric, Papp, Jeanette
Formato: Artigo
Idioma:Inglês
Publicado em: 2009
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2714875/
https://ncbi.nlm.nih.gov/pubmed/19574904
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/ICO.0b013e31819672fb
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