Papers

Peer-reviewed
Dec, 2016

A novel splice site mutation in the ADAR gene leading to exon skipping and dyschromatosis symmetrica hereditaria in a Japanese patient

CLINICAL AND EXPERIMENTAL DERMATOLOGY
  • O. Ansai
  • ,
  • Y. Shigehara
  • ,
  • A. Ito
  • ,
  • R. Abe
  • ,
  • Y. Shimomura

Volume
41
Number
8
First page
933
Last page
934
Language
English
Publishing type
DOI
10.1111/ced.12981
Publisher
WILEY-BLACKWELL

Link information
DOI
https://doi.org/10.1111/ced.12981
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/27747905
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000388506000026&DestApp=WOS_CPL
ID information
  • DOI : 10.1111/ced.12981
  • ISSN : 0307-6938
  • eISSN : 1365-2230
  • Pubmed ID : 27747905
  • Web of Science ID : WOS:000388506000026

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