Six novel mutations of theADAR1gene in patients with dyschromatosis symmetrica hereditaria: Histological observation and comparison of genotypes and clinical phenotypes-Reference-Cited by-同舟云学术

Six novel mutations of theADAR1gene in patients with dyschromatosis symmetrica hereditaria: Histological observation and comparison of genotypes and clinical phenotypes

Published:2008-07 Issue:7 Volume:35 Page:395-406
ISSN:0385-2407
Container-title:The Journal of Dermatology
language:en
Short-container-title:

Author:

KONDO Taisuke,SUZUKI Tamio,MITSUHASHI Yoshihiko,ITO Shiro,KONO Michihiro,KOMINE Mayumi,AKITA Hirotaka,TOMITA Yasushi

Publisher

Wiley

Subject

Dermatology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1346-8138.2008.00493.x/fullpdf

Reference46 articles.

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3. An unknown disorder of hyperpigmentation (in Japanese);Toyama;Jpn J Dermatol Urol,1910

4. Dyschromatosis symmetrica hereditaria (in Japanese);Toyama;Jpn J Dermatol Urol,1929

5. Mutations of the RNA-specific adenosine deaminase gene (DSRAD) are involved in dyschromatosis symmetrica hereditaria;Miyamura;Am J Hum Genet,2003

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1. Identification of five novel variants of ADAR1 in dyschromatosis symmetrica hereditaria by next-generation sequencing;Frontiers in Pediatrics;2023-07-05

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5. A case of dyschromatosis symmetrica hereditaria with an associated eyelid hemangioma;International Journal of Surgery Case Reports;2021-02