Ultrastructural Changes Resulting from Keratin-9 Gene Mutations in Two Families with Epidermolytic Palmoplantar Keratoderma
- 1 March 1995
- journal article
- Published by Elsevier in Journal of Investigative Dermatology
- Vol. 104 (3) , 425-429
- https://doi.org/10.1111/1523-1747.ep12666011
Abstract
No abstract availableKeywords
This publication has 28 references indexed in Scilit:
- Tylosis oesophageal cancer mappedNature Genetics, 1994
- Filaggrin expression in epidermolytic ichthyosis (epidermolytic hyperkeratosis)British Journal of Dermatology, 1994
- The hereditary palmoplantar keratoses: an updated review and classificationBritish Journal of Dermatology, 1994
- Molecular characterization of the body site-specific human epidermal cytokeratin 9: cDNA cloning, amino acid sequence, and tissue specificity of gene expressionDifferentiation, 1993
- Identification of the genetic locus for keratosis palmaris et plantaris on chromosome 17 near the RARA and keratin type I genesNature Genetics, 1993
- A Keratin 14 Mutational Hot Spot for Epidermolysis Bullosa Simplex, Dowling-Meara: Implications for DiagnosisJournal of Investigative Dermatology, 1993
- Keratin Intermediate Filament StructureJournal of Molecular Biology, 1993
- Hereditary epidermolytic palmoplantar keratoderma associated with breast and ovarian cancer in a large kindredBritish Journal of Dermatology, 1987
- Epidermolytic hereditary palmoplantar keratoderma.British Journal of Dermatology, 1978
- Zur Kenntniss des Keratoma hereditarium palmare et plantareArchives of Dermatological Research, 1901