1. Bukhari IA, El-Harith EA, Stuhrmann M. Dyschromatosis universalis hereditaria as an autosomal recessive disease in five members of one family. J Eur Acad Dermatol Venereol. 2006; 20:628–629.
Article
2. Sethuraman G, Srinivas CR, D'Souza M, Thappa DM, Smiles L. Dyschromatosis universalis hereditaria. Clin Exp Dermatol. 2002; 27:477–479.
Article
3. Kim NS, Im S, Kim SC. Dyschromatosis universalis hereditaria: an electron microscopic examination. J Dermatol. 1997; 24:161–164.
Article
4. Liu H, Li Y, Hung KK, Wang N, Wang C, Chen X, et al. Genome-wide linkage, exome sequencing and functional analyses identify ABCB6 as the pathogenic gene of dyschromatosis universalis hereditaria. PLoS One. 2014; 9:e87250.
Article
5. Ro YS, Nam TS, Lee CW, Park CK, Seou WP, Kim JH. Dyschromatosis universalis hereditaria. Ann Dermatol. 1990; 2:24–30.
Article