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added after printed version of Acta Derm Venereol 2007; 87: 459–480 Acta Derm Venereol 87 5. Herz C, Aumailley M, Schulte C, Schlotzer-Schrehardt U, Bruckner-Tuderman L, Has C. Kindlin-1 is a phosphopro-tein involved in regulation of polarity, proliferation, and motility of epidermal keratinocytes. J Biol Chem 2006; 281: 36082–36090.6. Kloeker S, Major MB, Calderwood DA, Ginsberg MH, Jones DA, Beckerle MC. The Kindler syndrome protein is regulated by transforming growth factor-beta and involved in integrin-mediated adhesion. J Biol Chem 2004; 279: 6824–6833.7. White SJ, McLean WH. Kindler surprise: mutations in a novel actin-associated protein cause Kindler syndrome. J Dermatol Sci 2005; 38: 169–175.8. Shimizu H, Sato M, Ban M, Kitajima Y, Ishizaki S, Harada T, et al. Immunohistochemical, ultrastructural, and mo-lecular features of Kindler syndrome distinguish it from dystrophic epidermolysis bullosa. Arch Dermatol 1997; 133: 1111–1117.9. Binder B, Metze D, Smolle J. Kongenitale bullose Poikilo-dermie (Kindler-Syndrom). Hautarzt 2002; 53: 546–549. 10. Ashton GH, McLean WH, South AP, Oyama N, Smith FJ, Al Suwaid R, et al. Recurrent mutations in kindlin-1, a novel keratinocyte focal contact protein, in the autosomal reces-sive skin fragility and photosensitivity disorder, Kindler syndrome. J Invest Dermatol 2004; 122: 78–83.11. Sethuraman G, Fassihi H, Ashton GH, Bansal A, Kabra M, Sharma VK, McGrath JA. An Indian child with Kindler syndrome resulting from a new homozygous nonsense mutation (C468X) in the KIND1 gene. Clin Exp Dermatol 2005; 30: 286–288.12. Burch JM, Fassihi H, Jones CA, Mengshol SC, Fitzpatrick JE, McGrath JA. Kindler syndrome: a new mutation and new diagnostic possibilities. Arch Dermatol 2006; 142: 620–624.13. Has C, Wessagowit V, Pascucci M, Baer C, Didona B, Wilhelm C, et al. Molecular basis of Kindler syndrome in Italy: novel and recurrent Alu/Alu recombination, splice site, nonsense, and frameshift mutations in the KIND1 gene. J Invest Dermatol 2006; 126: 1776–1783.14. Sadler E, Klausegger A, Muss W, Deinsberger U, Pohla-Gubo G, Laimer M, et al. Novel KIND1 Gene mutation in Kindler syndrome with severe gastrointestinal tract invol-vement. Arch Dermatol 2006; 142: 1619–1624.15. Thomson MA, Ashton GH, McGrath JA, Eady RA, Moss C. Retrospective diagnosis of Kindler syndrome in a 37-year-old man. Clin Exp Dermatol 2006; 31: 45–47.

Novel and Recurrent KIND1 Mutations in Two Patients with Kindler Syndrome and Severe Mucosal Involvement