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Exclusion of known corneal dystrophy genes in an autosomal dominant pedigree of a unique anterior membrane corneal dystrophy

PURPOSE: With advances in phenotyping tools and availability of molecular characterization, an increasing number of phenotypically and genotypically diverse inherited corneal dystrophies are described. We aimed to determine the underlying causative genetic mechanism in a three-generation pedigree af...

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Detaylı Bibliyografya
Asıl Yazarlar: Vincent, Andrea L., Markie, David M., De Karolyi, Betina, Wheeldon, Catherine E., Patel, Dipika V., Grupcheva, Christina N., McGhee, Charles N.J.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Molecular Vision 2009
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC2731832/
https://ncbi.nlm.nih.gov/pubmed/19710953
Etiketler: Etiketle
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