A novel mutation of the Keratin 12 gene responsible for a severe phenotype of Meesmann's corneal dystrophy

PURPOSE: To determine if a mutation within the coding region of the keratin 12 gene (KRT12) is responsible for a severe form of Meesmann's corneal dystrophy. METHODS: A family with clinically identified Meesmann's corneal dystrophy was recruited and studied. Electron microscopy was perform...

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Main Authors: Sullivan, Lori S., Baylin, Eric B., Font, Ramon, Daiger, Stephen P., Pepose, Jay S., Clinch, Thomas E., Nakamura, Hisashi, Zhao, Xinping C., Yee, Richard W.
Formato: Artigo
Idioma:Inglês
Publicado em: Molecular Vision 2007
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2774455/
https://ncbi.nlm.nih.gov/pubmed/17653038
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