Meesmann Corneal Dystrophy (MECD): Report of 2 Families and a Novel Mutation in the Cornea Specific Keratin 12 ( KRT12 ) Gene

Author： Nichini Olivia   Manzi Violaine   Munier Francis   Schorderet Daniel  

Publisher： Informa Healthcare

ISSN： 1381-6810

Source： Ophthalmic Genetics, Vol.26, Iss.4, 2005-12, pp. : 169-173

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