1. Al-Imara L, Richards AJ, Eady RA, Leigh IM, Farrall M, Pope HM. Linkage of autosomal dominant dystrophic epidermolysis bullosa in three British families to the marker D3S2, close to the COL7A1 locus. J Med Genet. 1992;29:381–2.
2. Anton-Lamprecht I, Hashimoto I. Epidermolysis bullosa dystrophica dominans (Pasini) – a primary structural defect of the anchoring fibrils. Hum Genet. 1976;32(1):69–76.
3. Bibhuti BD, Sunati S. Dystrophic epidermolysis bullosa. J Perinatol. 2004;24:41–7.
4. Christiano AM, McGrath JA, Tan KC, Uitto J. Glycine substitutions in the triple-helical region of type VII collagen result in a spectrum of dystrophic epidennolysis bullosa phenotypes and patterns of inheritance. Am J Hum Genet. 1996;58:671–81.
5. Eady RAJ. Current perspectives and differential diagnosis in epidermolysis bullosa. In: Lin AN, Carter DM, editors. Epidermolysis bullosa: basic and clinical aspects. New York: Springer; 1992. p. 3–15.