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Heterozygous mutations affecting the protein kinase domain of CDK13 cause a syndromic form of developmental delay and intellectual disability.
scientific article
Author/s
author: Richard Caswell, Mark J Hamilton, Ketil R. Heimdal, Emma Wakeling, Andrew Oliver Mungo Wilkie, Stephen Twigg, Helen Firth, Ruth Newbury-Ecob
Work details
Publication date
October 11, 2017
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Language
English
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