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Dyschromatosis symmetrica hereditaria with chilblains due to a novel two‐amino‐acid deletion in the double‐stranded RNA‐binding domain of ADAR1

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Published in:	Journal of the European Academy of Dermatology and Venereology 2018-10, Vol.32 (10), p.e394-e396
Main Authors:	Kono, M., Suganuma, M., Shimada, T., Ishikura, Y., Watanabe, S., Takeichi, T., Muro, Y., Akiyama, M.
Format:	Article
Language:	English
Subjects:	Adenosine Deaminase - genetics Base Sequence Chilblains - complications Chilblains - genetics Child Double-Stranded RNA Binding Motif - genetics Female Humans Pedigree Pigmentation Disorders - complications Pigmentation Disorders - congenital Pigmentation Disorders - genetics Pigmentation Disorders - pathology RNA-Binding Proteins - genetics Sequence Deletion
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container_title	Journal of the European Academy of Dermatology and Venereology
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creator	Kono, M. Suganuma, M. Shimada, T. Ishikura, Y. Watanabe, S. Takeichi, T. Muro, Y. Akiyama, M.
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doi_str_mv	10.1111/jdv.15076
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identifier	ISSN: 0926-9959
ispartof	Journal of the European Academy of Dermatology and Venereology, 2018-10, Vol.32 (10), p.e394-e396
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source	Wiley-Blackwell Read & Publish Collection
subjects	Adenosine Deaminase - genetics Base Sequence Chilblains - complications Chilblains - genetics Child Double-Stranded RNA Binding Motif - genetics Female Humans Pedigree Pigmentation Disorders - complications Pigmentation Disorders - congenital Pigmentation Disorders - genetics Pigmentation Disorders - pathology RNA-Binding Proteins - genetics Sequence Deletion
title	Dyschromatosis symmetrica hereditaria with chilblains due to a novel two‐amino‐acid deletion in the double‐stranded RNA‐binding domain of ADAR1
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