Mutations in the γ2 chain gene (LAMC2) of kalinin/laminin 5 in the junctional forms of epidermolysis bullosa
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics
Link
http://www.nature.com/articles/ng0394-293.pdf
Reference43 articles.
1. Lin, A.N. & Carter, D.M. (eds) Epidermolysis bullosa. Basic and clinical aspects (Springer-Verlag, New York, 1992).
2. Fine, J.D. et al. Revised clinical and laboratory criteria for subtypes of inherited epidermolysis bullosa. A consensus report by the subcommittee on diagnosis and classification of the National Epidermolysis Bullosa Registry. J. Am. Acad. Dermatol. 24, 119–135 (1991).
3. Epstein, E.H., Jr. Molecular genetics of epidermolysis bullosa. Science 256, 799–804 (1992).
4. Uitto, J. & Christiano, A.M. Molecular genetics of the cutaneous basement membrane zone. Perspectives on epidermolysis bullosa and other blistering skin diseases. J. clin. Invest. 90, 687–692 (1992).
5. Bonifas, J.M., Rothman, A.-L. & Epstein, E. Epidermolysis bullosa simplex: evidence in two families for keratin gene abnormalities. Science 254, 1201–1205 (1991).
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