A novel microdeletion in LOR causing autosomal dominant loricrin keratoderma. (1st January 2015) - Kinsler, V.A.; Drury, S.; Khan, A.; Waelchli, R.; Rukaite, G.; Barnicoat, A.; Lench, N.; Harper, J.I.; O'Shaughnessy, R.F.L.