Citations for
1LOR, PSEK1
Evidence for the absence of mutations at GJB3, GJB4 and LOR in progressive symmetrical erythrokeratodermia.
Wei S, Zhou Y, Zhang TD, Huang ZM, Zhang XB, Zhu HL, Liang BH, Lin L, Deng L.
Clin Exp Dermatol 36(4):399-405. doi: 10.1111/j.1365-2230.2010.03974.x. Epub 2010 Dec 24. 2011
2LOR, PSEK1
The molecular pathology of progressive symmetric erythrokeratoderma: a frameshift mutation in the loricrin gene and perturbations in the cornified cell envelope.
Ishida-Yamamoto A, McGrath JA, Lam H, Iizuka H, Friedman RA, Christiano AM.
Am J Hum Genet 61(3):581-9. 1997
3PSEK1
Is erythrokeratoderma one disorder? A clinical and ultrastructural study of two siblings.
Macfarlane AW, Chapman SJ, Verbov JL.
Br J Dermatol 124(5):487-91. 1991