A Missense Mutation in the Cadherin Interaction Site of The Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- 1 November 2005
- journal article
- Published by Elsevier in Journal of Investigative Dermatology
- Vol. 125 (5) , 1077-1079
- https://doi.org/10.1111/j.0022-202x.2005.23903.x
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- A spontaneous mutation in the desmoglein 4 gene underlies hypotrichosis in a new lanceolate hair rat modelDifferentiation, 2004
- Intragenic deletion in the Desmoglein 4 gene underlies the skin phenotype in the Iffa Credo “hairless” ratDifferentiation, 2004
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive HypotrichosisJournal of Investigative Dermatology, 2004
- A Recurrent Intragenic Deletion Mutation in DSG4 Gene in Three Pakistani Families with Autosomal Recessive HypotrichosisJournal of Investigative Dermatology, 2004
- The lanceolate hair rat phenotype results from a missense mutation in a calcium coordinating site of the desmoglein 4 geneGenomics, 2004
- Cadherin-mediated cell–cell adhesion: sticking together as a familyCurrent Opinion in Structural Biology, 2003
- A locus for hereditary hypotrichosis localized to human chromosome 18q21.1European Journal of Human Genetics, 2003
- Desmoglein 4 in hair follicle differentiation and epidermal adhesion: evidence from inherited hypotrichosis and acquired pemphigus vulgaris.Published by Elsevier ,2003
- C-Cadherin Ectodomain Structure and Implications for Cell Adhesion MechanismsScience, 2002
- Structure-Function Analysis of Cell Adhesion by Neural (N-) CadherinNeuron, 1998