2Lamartine J, Munhoz Essenfelder G, Kibar Z, et al. Mutations in GJB6 cause hidrotic ectodermal dysplasia. Nat Genet 2000;26(2): 142- 144.
3Van Steensel MA, Steijlen PM, Bladergroen RS, et al. A pheno-type resembling the Clouston syndrome with deafness is associated with a novel missense GJB2 mutation. J Invest Dermatol 2004; 123 (2) :291 - 293. S243.
4Hart PS, Zhang Y, Firatli E, et al. Identification of cathepsin C mutations in edmically diverse Paillon- Lefevre syndrome patients. J Med Genet 2000; 37: 927 - 932.
5Clouston HR. A hereditary ectodermal dystrophy. Canad Med Assoc 1929;21(1) : 18 - 31.
6Nan CHEN, Chao XU, Bing HAN, et al. G11R mutation in GJB6 gene causes hidrotic ectodermal dysplasia involving only hair and nails in a Chinese family. J Dermatol 2010;37:1 -3.
7Baris HN, Zlotogorski A, Peretz - Amit G, et al. A novel GJB6 missense mutation in hidrotic ectodermal dysplasia (Clouston syn- drome) broadens its genotypic basis. Br J Dermatol 2008; 159(6) : 1373- 1376.
