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Mutation analysis of the ADAR1 gene in dyschromatosis symmetrica hereditaria and genetic differentiation from both dyschromatosis universalis hereditaria and acropigmentatio reticularis.
Suzuki N, Suzuki T, Inagaki K, Ito S, Kono M, Fukai K, Takama H, Sato K, Ishikawa O, Abe M, Shimizu H, Kawai M, Horikawa T, Yoshida K, Matsumoto K, Terui T, Tsujioka K, Tomita Y. Suzuki N, et al. Among authors: horikawa t. J Invest Dermatol. 2005 Jun;124(6):1186-92. doi: 10.1111/j.0022-202X.2005.23732.x. J Invest Dermatol. 2005. PMID: 15955093
Association of a mutation in TRPV3 with defective hair growth in rodents.
Asakawa M, Yoshioka T, Matsutani T, Hikita I, Suzuki M, Oshima I, Tsukahara K, Arimura A, Horikawa T, Hirasawa T, Sakata T. Asakawa M, et al. Among authors: horikawa t. J Invest Dermatol. 2006 Dec;126(12):2664-72. doi: 10.1038/sj.jid.5700468. Epub 2006 Jul 20. J Invest Dermatol. 2006. PMID: 16858425
Single, blue nevus-like localized argyria.
Nagano T, Oka M, Horikawa T, Nishigori C, Kotera M. Nagano T, et al. Among authors: horikawa t. J Dermatol. 2016 Nov;43(11):1359-1360. doi: 10.1111/1346-8138.13387. Epub 2016 Apr 20. J Dermatol. 2016. PMID: 27094929 No abstract available.
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