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Original research
Telangiectasia-ectodermal dysplasia-brachydactyly-cardiac anomaly syndrome is caused by de novo mutations in protein kinase D1
- Correspondence to Professor Dr Judith Fischer, Institute for Human Genetics, Medical Center – University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany; judith.fischer{at}uniklinik-freiburg.de; Professor Susan F Steinberg, Department of Pharmacology, Columbia University, New York, New York, USA; sfs1{at}cumc.columbia.edu
Citation
Telangiectasia-ectodermal dysplasia-brachydactyly-cardiac anomaly syndrome is caused by de novo mutations in protein kinase D1
Publication history
- Received December 20, 2019
- Revised May 18, 2020
- Accepted May 30, 2020
- First published August 17, 2020.
Online issue publication
May 21, 2021
Article Versions
- Previous version (17 August 2020).
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© Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ.