Ten Novel Mutations of the ADAR1 Gene in Japanese Patients with Dyschromatosis Symmetrica Hereditaria-Reference-Cited by-同舟云学术

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

Published:2007-02 Issue:2 Volume:127 Page:309-311
ISSN:0022-202X
Container-title:Journal of Investigative Dermatology
language:en
Short-container-title:Journal of Investigative Dermatology

Author:

Suzuki Noriyuki,Suzuki Tamio,Inagaki Katsuhiko,Ito Shiro,Kono Michihiro,Horikawa Tatsuya,Fujiwara Sakuhei,Ishiko Akira,Matsunaga Kayoko,Aoyama Yumi,Tosaki-Ichikawa Hiroko,Tomita Yasushi

Publisher

Elsevier BV

Subject

Cell Biology,Dermatology,Molecular Biology,Biochemistry

Reference14 articles.

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2. A novel deletion mutation of the DSRAD gene in a Taiwanese patient with dyschromatosis symmetrica hereditaria;Chao;Br J Dermatol,2005

3. Identification of a novel mutation in the DSRAD gene in a Chinese pedigree with dyschromatosis symmetrica hereditaria;Cui;Arch Dermatol Res,2005

4. Human RNA-specific adenosine deaminase (ADAR1) gene specifies transcripts that initiate from a constitutively active alternative promoter;Kawakubo;Gene,2000

5. A new arginine substitution mutation of DSRAD gene in a Chinese family with dyschromatosis symmetrica hereditaria;Li;J Dermatol Sci,2005

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