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Title
A novel arginine substitution mutation in 1A domain and a novel 27 bp insertion mutation in 2B domain of keratin 12 gene associated with Meesmann's corneal dystrophy.
Authors
Yoon, M K; Warren, J F; Holsclaw, D S; Gritz, D C; Margolis, T P
Abstract
To determine the disease causing gene defects in two patients with Meesmann's corneal dystrophy.
Publication
The British journal of ophthalmology, 2004, Vol 88, Issue 6, p752