Epidermolysis bullosa simplex: a disorder of keratin
- 4 January 1992
- journal article
- editorial
- Published by Elsevier in The Lancet
- Vol. 339 (8784) , 29-30
- https://doi.org/10.1016/0140-6736(92)90147-u
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
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- Mutant keratin expression in transgenic mice causes marked abnormalities resembling a human genetic skin diseaseCell, 1991
- Revised clinical and laboratory criteria for subtypes of inherited epidermolysis bullosaJournal of the American Academy of Dermatology, 1991
- Expression of mutant keratin cDNAs in epithelial cells reveals possible mechanisms for initiation and assembly of intermediate filaments.The Journal of cell biology, 1989
- Functions of intermediate filamentsCell Motility, 1989
- Regulated expression of differentiation-associated keratins in cultured epidermal cells detected by monospecific antibodies to unique peptides of mouse epidermal keratinsDifferentiation, 1987