Keratotic lesions in epidermolysis bullosa simplex with mottled pigmentation
Open Access
- 31 January 2005
- journal article
- research article
- Published by Elsevier in Journal of the American Academy of Dermatology
- Vol. 52 (1), 172-173
- https://doi.org/10.1016/j.jaad.2004.07.046
Abstract
No abstract availableKeywords
This publication has 4 references indexed in Scilit:
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- N-terminal deletion in a desmosomal cadherin causes the autosomal dominant skin disease striate palmoplantar keratodermaHuman Molecular Genetics, 1999
- The genetic basis of epidermolysis bullosa simplex with mottled pigmentation.Proceedings of the National Academy of Sciences, 1996
- Making a connection: direct binding between keratin intermediate filaments and desmosomal proteins.The Journal of cell biology, 1994