Getting under the skin
- 1 November 1991
- journal article
- Published by Springer Nature in Nature
- Vol. 354 (6351) , 264-265
- https://doi.org/10.1038/354264a0
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
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- Point mutations in human keratin 14 genes of epidermolysis bullosa simplex patients: Genetic and functional analysesCell, 1991
- Epidermolysis Bullosa Simplex (Koebner) Is a Keratin DisorderArchives of Dermatology, 1991
- Mutant keratin expression in transgenic mice causes marked abnormalities resembling a human genetic skin diseaseCell, 1991
- Functions of intermediate filamentsCell Motility, 1989
- Functional inactivation of genes by dominant negative mutationsNature, 1987