2Drera B. De novo occurrence of the 730insG recurrent mutation in an Italian family with the ichthyotic variant of Vohwinkel syndrome, Loricrin keratoderma. Clin Genet 2008 ; 73 : 85 - 88.
3Amstrong DK. A novel insertional mutation in loricrin in Vohwinkel' s keratoderma. J Invest Dermatol 1998 ; 111 : 702 - 704.
4Snoeckx R. Mutation analysis of the GJB2 (connexin 26) gene in Egypt. Hum Mutat 2005;26:60- 61.
5Richard G, Brown N, Smith LE, et al. The spectrum of mutations in eokeratodennias - novel and de novo mutations in GJB3. Hum Genet 2000; 106(3) :321 - 329.