Article info

Short report
A complex DICER1 syndrome phenotype associated with a germline pathogenic variant affecting the RNase IIIa domain of DICER1

Authors

  1. Correspondence to Professor Ann Nordgren, Dept of Molecular Medicine and Surgery (MMK), Karolinska Institute, 171 64 Stockholm, Sweden; ann.nordgren{at}ki.se
View Full Text

Citation

Pontén E, Frisk S, Taylan F, et al
A complex DICER1 syndrome phenotype associated with a germline pathogenic variant affecting the RNase IIIa domain of DICER1

Publication history

  • Received August 5, 2020
  • Revised October 10, 2020
  • Accepted October 12, 2020
  • First published November 18, 2020.
  • Supplementary Data

    This web only file has been produced by the BMJ Publishing Group from an electronic file supplied by the author(s) and has not been edited for content.

Request permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.