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Klinische Monatsblatter Fur Augenheilkunde|May 13, 1998
[Progressive disseminated essential telangiectasia with conjunctival involvement]B Swensson, O Swensson, G HäringKlinische Monatsblatter Fur Augenheilkunde|August 19, 2000
[Mutations in the keratin gene as a cause of Meesman-Wilke corneal dystrophy and autosomal dominant skin cornification disorders]O Swensson, B Swensson, B Nölle, et al.Experimental Eye Research|January 25, 2000
Molecular genetics of Meesmann's corneal dystrophy: ancestral and novel mutations in keratin 12 (K12) and complete sequence of the human KRT12 geneL D Corden, O Swensson, B Swensson, et al.The British Journal of Ophthalmology|April 27, 2000
A novel keratin 12 mutation in a German kindred with Meesmann's corneal dystrophyL D Corden, O Swensson, B Swensson, et al.Nature Genetics|June 1, 1997
Mutations in cornea-specific keratin K3 or K12 genes cause Meesmann's corneal dystrophyA D Irvine, L D Corden, O Swensson, et al.Pageof 1