Heterozygous mutations affecting the protein kinase domain of CDK13 cause a syndromic form of developmental delay and intellectual disability
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K. Heimdal | Soo-Mi Park | H. Firth | S. Twigg | A. Wilkie | Dhavendra Kumar | R. Newbury-Ecob | N. Canham | G. Houge | R. Caswell | T. Cole | N. Foulds | I. Maystadt | E. Hobson | S. Joss | A. Lampe | K. Metcalfe | L. Robert | M. Suri | E. Wakeling | M. Hamilton | C. Rustad | V. McKay | The Deciphering Developmental Disorders Study | T. Cole