We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleMeesmann corneal dystrophy (MECD): report of 2 families and a novel mutation in the cornea specific keratin 12 (KRT12) gene.AuthorsNichini O; Manzi Vd; Munier FL; Schorderet DFPublicationOphthalmic genetics, 2005, Vol 26, Issue 4, p169ISSN1381-6810Publication typearticleDOI10.1080/13816810500374391