Spectrum of dominant mutations in the desmosomal cadherin desmoglein 1, causing the skin disease striate palmoplantar keratoderma
Open Access
- 1 March 2001
- journal article
- research article
- Published by Springer Nature in European Journal of Human Genetics
- Vol. 9 (3), 197-203
- https://doi.org/10.1038/sj.ejhg.5200605
Abstract
No abstract availableKeywords
This publication has 40 references indexed in Scilit:
- Clustered Cadherin Genes: A Sequence-Ready Contig for the Desmosomal Cadherin Locus on Human Chromosome 18Genomics, 1999
- Striate Palmoplantar Keratoderma Resulting from Desmoplakin HaploinsufficiencyJournal of Investigative Dermatology, 1999
- N-terminal deletion in a desmosomal cadherin causes the autosomal dominant skin disease striate palmoplantar keratodermaHuman Molecular Genetics, 1999
- The palmoplantar keratodermas: much more than palms and solesMolecular Medicine Today, 1999
- Haploinsufficiency of desmoplakin causes a striate subtype of palmoplantar keratoderma [published erratum appears in Hum Mol Genet 1999 May;8(5):943]Human Molecular Genetics, 1999
- Aspects of the structure and assembly of desmosomesMicron, 1998
- Desmosomes: Intercellular Adhesive Junctions Specialized for Attachment of Intermediate FilamentsInternational Review of Cytology, 1998
- Linkage of an American Pedigree With Palmoplantar Keratoderma and Malignancy (Palmoplantar Ectodermal Dysplasia Type III) to 17q24Archives of Dermatology, 1996
- Localization of a locus for the striated form of palmoplantar keratoderma to chromosome 18q near the desmosomal cadherin gene clusterHuman Molecular Genetics, 1995
- Chromosomal assignment of the human genes coding for the major proteins of the desmosome junction, desmoglein DGI (DSG), desmocollins
DGII III DPI II Genomics, 1991