A novel keratin 12 mutation in a German kindred with Meesmann's corneal dystrophy

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• Allele-specific siRNA silencing for the common Keratin 12 founder mutation in Meesmann epithelial corneal dystrophy
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• Keratin 12 missense mutation induces the unfolded protein response and apoptosis in Meesmann epithelial corneal dystrophy
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• Identification of a novel mutation in the cornea specific keratin 12 gene causing Meesmann`s corneal dystrophy in a German family
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• A novel mutation of the Keratin 12 gene responsible for a severe phenotype of Meesmann's corneal dystrophy
  per: Sullivan, Lori S., et al.
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