A Recurrent Intragenic Deletion Mutation in DSG4 Gene in Three Pakistani Families with Autosomal Recessive Hypotrichosis
Open Access
- 1 July 2004
- journal article
- Published by Elsevier in Journal of Investigative Dermatology
- Vol. 123 (1), 247-248
- https://doi.org/10.1111/j.0022-202x.2004.22715.x
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- A locus for hereditary hypotrichosis localized to human chromosome 18q21.1European Journal of Human Genetics, 2003
- Desmoglein Isotype Expression in the Hair Follicle and its Cysts Correlates with Type of Keratinization and Degree of DifferentiationJournal of Investigative Dermatology, 2003
- Genomic Sequence Analysis of the Mouse Desmoglein Cluster Reveals Evidence for Six Distinct Genes: Characterization of Mouse DSG4, DSG5, and DSG6Journal of Investigative Dermatology, 2003
- Genetic Evidence for a Novel Human Desmosomal Cadherin, Desmoglein 4Journal of Investigative Dermatology, 2003
- Desmoglein 4 in Hair Follicle Differentiation and Epidermal AdhesionCell, 2003
- Cloning of the Gene for Human Pemphigus Vulgaris Antigen (Desmoglein 3), a Desmosomal CadherinPublished by Elsevier ,1996
- The structural and functional analysis of cadherin calcium-dependent cell adhesion moleculesCurrent Opinion in Cell Biology, 1993
- Human globin locus activation region (LAR): role in temporal controlTrends in Genetics, 1990
- Characterization of Pemphigus Foliaceus Antigen from Human EpidermisJournal of Investigative Dermatology, 1990