The Okur-Chung Neurodevelopmental Syndrome Mutation CK2K198R Leads to a Rewiring of Kinase Specificity.

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Bibliographic Details
Title: The Okur-Chung Neurodevelopmental Syndrome Mutation CK2K198R Leads to a Rewiring of Kinase Specificity.
Authors: Caefer DM; Department of Physiology and Neurobiology, University of Connecticut, Storrs, CT, United States., Phan NQ; Department of Physiology and Neurobiology, University of Connecticut, Storrs, CT, United States., Liddle JC; Center for Open Research Resources and Equipment, Proteomics and Metabolomics Facility, University of Connecticut, Storrs, CT, United States., Balsbaugh JL; Center for Open Research Resources and Equipment, Proteomics and Metabolomics Facility, University of Connecticut, Storrs, CT, United States., O'Shea JP; Department of Physiology and Neurobiology, University of Connecticut, Storrs, CT, United States., Tzingounis AV; Department of Physiology and Neurobiology, University of Connecticut, Storrs, CT, United States., Schwartz D; Department of Physiology and Neurobiology, University of Connecticut, Storrs, CT, United States.
Source: Frontiers in molecular biosciences [Front Mol Biosci] 2022 Apr 19; Vol. 9, pp. 850661. Date of Electronic Publication: 2022 Apr 19 (Print Publication: 2022).
Publication Type: Journal Article
Journal Info: Publisher: Frontiers Media S.A Country of Publication: Switzerland NLM ID: 101653173 Publication Model: eCollection Cited Medium: Print ISSN: 2296-889X (Print) Linking ISSN: 2296889X NLM ISO Abbreviation: Front Mol Biosci Subsets: PubMed not MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:2296-889X
DOI:10.3389/fmolb.2022.850661