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Genetic analyses of oculocutaneous albinism types 2 and 4 with eight novel mutations.
Okamura K, Araki Y, Abe Y, Shigyou A, Fujiyama T, Baba A, Kanekura T, Chinen Y, Kono M, Niizeki H, Tsubota A, Konno T, Hozumi Y, Suzuki T. Okamura K, et al. Among authors: suzuki t. J Dermatol Sci. 2016 Feb;81(2):140-2. doi: 10.1016/j.jdermsci.2015.10.014. Epub 2015 Oct 31. J Dermatol Sci. 2016. PMID: 26573111 No abstract available.
Oculocutaneous albinism type 4 is one of the most common types of albinism in Japan.
Inagaki K, Suzuki T, Shimizu H, Ishii N, Umezawa Y, Tada J, Kikuchi N, Takata M, Takamori K, Kishibe M, Tanaka M, Miyamura Y, Ito S, Tomita Y. Inagaki K, et al. Among authors: suzuki t. Am J Hum Genet. 2004 Mar;74(3):466-71. doi: 10.1086/382195. Epub 2004 Feb 11. Am J Hum Genet. 2004. PMID: 14961451 Free PMC article.
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: suzuki 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 Free article.
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