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Original Article
Heterozygous mutations affecting the protein kinase domain of CDK13 cause a syndromic form of developmental delay and intellectual disability

Authors

  1. Correspondence to Dr Mohnish Suri, Consultant Clinical Geneticist, Nottingham City Hospital, Hucknall Road, Nottingham, Nottinghamshire NG5 1PB, UK; mohnish.suri{at}nhs.net
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Citation

Hamilton MJ, Caswell RC, Canham N, et al
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.

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