Mutations in the 1A Domain of Keratin 9 in Patients with Epidermolytic Palmoplantar Keratoderma
- 1 March 1995
- journal article
- Published by Elsevier in Journal of Investigative Dermatology
- Vol. 104 (3) , 430-433
- https://doi.org/10.1111/1523-1747.ep12666018
Abstract
No abstract availableKeywords
This publication has 27 references indexed in Scilit:
- Mutations of Keratin 9 in Two Families with Palmoplantar Epidermolytic HyperkeratosisJournal of Investigative Dermatology, 1994
- Epidermal disease: faulty keratin filaments take their tollNature Genetics, 1994
- Molecular characterization of the body site-specific human epidermal cytokeratin 9: cDNA cloning, amino acid sequence, and tissue specificity of gene expressionDifferentiation, 1993
- A Keratin 14 Mutational Hot Spot for Epidermolysis Bullosa Simplex, Dowling-Meara: Implications for DiagnosisJournal of Investigative Dermatology, 1993
- Keratin Intermediate Filament Structure: Crosslinking Studies Yield Quantitative Information on Molecular Dimensions and Mechanism of AssemblyJournal of Molecular Biology, 1993
- Hereditary epidermolytic palmo-plantar keratoderma (Vorner type)-report of a family and review of the literatureClinical and Experimental Dermatology, 1991
- Cytokeratin No. 9, an epidermal type I keratin characteristic of a special program of keratinocyte differentiation displaying body site specificity.The Journal of cell biology, 1986
- Patterns of Expression and Organization of Cytokeratin Intermediate FilamentsAnnals of the New York Academy of Sciences, 1985
- Hereditary callosities with blisters: Report of a family and reviewPublished by Elsevier ,1984
- Zur Kenntniss des Keratoma hereditarium palmare et plantareArchives of Dermatological Research, 1901