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

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Description scientific article
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author: Mark J Hamilton  Ketil R. Heimdal  Emma Wakeling  Helen Firth  Stephen Twigg  Andrew Oliver Mungo Wilkie  Richard Caswell  Ruth Newbury-Ecob 

Publication date October 11, 2017
Language English
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