3Ferrando J, Galve J, Torres-Puente M, et al. Monilethrix: a new family with the novel mutation in KRT81 gene[J]. Int J Tfichology, 2012, 4( 1 ): 53-55.
4Schweizer J. More than one gene involved in monilethrix: intra- cellular but also extracellular players [J ]. J Invest Dermatol, 2006, 126(6): 1216-1219.
5Shimomura Y, Sakamoto F, Kariya N, et al. Mutations in the des- moglein 4 gene are associated with monilethrix-like congenital hypotrichosis [ J ]. J Invest Dermatol, 2006, 126(6): 1281-1285.
6Kljuic A, Bazzi H, Sundberg JP, et al. Desmoglein 4 in hair follicle differentiation and epidermal adhesion: evidence from inherited hypotrichosis and acquired pemphigus vulgaris [ J ]. Cell, 2003, 113 (2): 249-260.
7Whittock NV, Bower C. Genetic evidence for a novel human des- mosomal cadherin, desmoglein 4 [ J ]. J Invest Dermatol, 2003, 120 (4): 523-530.
8Zlotogorski A, Marek D, Horev L, et al. An autosomal recessive form of monilethrix is caused by mutations in DSG4: clinical overlap with localized autosomal recessive hypotrichosis [J]. J Invest Dermatol, 2006, 126(6): 1292-1296.
9Schaffer JV, Bazzi H, Vitebsky A, et al. Mutations in the desmoglein 4 gene underlie localized autosomal recessive hypotrichosis with monilethrix hairs and congenital scalp erosions [J]. J Invest Dermatol, 2006, 126(6): 1286-1291.
10Wajid M, Bazzi H, Rockey J, et al. Localized aut0somal recessive hypotrichosis due to a frameshift mutation in the desmoglein 4 gene exhibits extensive phenotypic variability within a Pakistani family [J]. J Invest Dermatol, 2007, 127(7): 1779-1782.
