Associated Papers
Mutations in the desmoglein 4 gene are associated with monilethrix-like congenital hypotrichosis.
Shimomura Y et al.
The Journal of Investigative Dermatology, 2006
Desmoglein 4 mutations underlie localized autosomal recessive hypotrichosis in humans, mice, and rats.
Bazzi H et al.
The Journal of Investigative Dermatology. Symposium Proceedings, 2005
Desmoglein 4 in hair follicle differentiation and epidermal adhesion: evidence from inherited hypotrichosis and acquired pemphigus vulgaris.
Kljuic A et al.
Cell, 2003
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