LAUSR

1. Fine JD, Bruckner-Tuderman L, Eady RA et al. Inherited epidermolysis bullosa: updated recommendations on diagnosis and classification. J. Am. Acad. Dermatol. 2014; 70: 1103–26. 2. Intong LR, Murrell DF. Inherited epidermolysis bullosa: new diagnostic criteria and classification. Clin. Dermatol. 2012; 30: 70–7. 3. Bolling MC, Lemmink HH, Jansen GH et al. Mutations in KRT5 and KRT14 cause epidermolysis bullosa simplex in 75% of the patients. Br. J. Dermatol. 2011; 164: 637–44. 4. Padalon-Brauch G, Ben Amitai D, Vodo D et al. Digenic inheritance in epidermolysis bullosa simplex. J. Invest. Dermatol. 2012; 132: 2852–4. 5. Wertheim-Tysarowska K, Sota J, Kutkowska-Ka zmierczak A et al. Coexistence of KRT14 and KRT5 mutations in a Polish patient with epidermolysis bullosa simplex. Br. J. Dermatol. 2014; 70: 468–9. 6. Wakiguchi H, Hasegawa S, Maeba S et al. A sporadic neonatal case of epidermolysis bullosa simplex generalized intermediate with KRT5 and KRT14 gene mutations. AJP Rep. 2016; 6: e108– 11. 7. Kim E, Harris A, Hyland V et al. Digenic inheritance in epidermolysis bullosa simplex involving two novel mutations in KRT5 and KRT14. Br. J. Dermatol. 2017; 177: 262–4. 8. Sch€ affer AA. Digenic inheritance in medical genetics. J. Med. Genet. 2013; 50: 641–52. 9. Knobel M, O'Toole EA, Smith FJ. Keratins and skin disease. Cell. Tissue. Res. 2015; 360: 583–9.