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Ten Novel Mutations of the ADAR1 Gene in Japanese Patients with Dyschromatosis Symmetrica Hereditaria

โœ Scribed by Suzuki, Noriyuki; Suzuki, Tamio; Inagaki, Katsuhiko; Ito, Shiro; Kono, Michihiro; Horikawa, Tatsuya; Fujiwara, Sakuhei; Ishiko, Akira; Matsunaga, Kayoko; Aoyama, Yumi


Book ID
110049601
Publisher
Nature Publishing Group
Year
2007
Tongue
English
Weight
93 KB
Volume
127
Category
Article
ISSN
0022-202X

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Seven novel mutations of the ADAR gene i
โœ Xue-Jun Zhang; Ping-Ping He; Ming Li; Chun-Di He; Kai-Lin Yan; Yong Cui; Sen Yan ๐Ÿ“‚ Article ๐Ÿ“… 2004 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 505 KB

Dyschromatosis symmetrica hereditaria (DSH) is an autosomal dominant pigmentary genodermatosis characterized by hyperpigmented and hypopigmented macules of on the extremities and caused by the mutations in the ADAR gene(also called DSRAD) encoding for RNA-specific adenosine deaminase. Here we report