Article info
New disease loci
Original Article
Heterozygous mutations affecting the protein kinase domain of CDK13 cause a syndromic form of developmental delay and intellectual disability
- Correspondence to Dr Mohnish Suri, Consultant Clinical Geneticist, Nottingham City Hospital, Hucknall Road, Nottingham, Nottinghamshire NG5 1PB, UK; mohnish.suri{at}nhs.net
Citation
Heterozygous mutations affecting the protein kinase domain of CDK13 cause a syndromic form of developmental delay and intellectual disability
Publication history
- Received February 23, 2017
- Revised September 4, 2017
- Accepted September 8, 2017
- First published October 11, 2017.
Online issue publication
December 15, 2017
Article Versions
- Previous version (11 October 2017).
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© Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted. This is an Open Access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 4.0) license, which permits others to distribute, remix, adapt and build upon this work, for commercial use, provided the original work is properly cited. See: http://creativecommons.org/licenses/by/4.0/