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

Author:

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

Publisher

Wiley

Subject

Dermatology,General Medicine

Reference46 articles.

1. Genetics of pigmentary disorders;Tomita;Am J Med Genet C Semin Med Genet,2004

2. Dyschromatosis symmetrica hereditaria (reticulate acropigmentation of Dohi): report of a Japanese family with the condition and a literature review of 185 cases;Oyama;Br J Dermatol,1999

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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