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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 23 February 2017
  • Revised 4 September 2017
  • Accepted 8 September 2017
  • Published online 11 October 2017.

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