Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Caefer DM"'
Autor:
Daniel Schwartz, Caefer Dm, Liddle Jc, O’Shea Jp, Phan Nq, Jeremy L. Balsbaugh, Anastasios V. Tzingounis
Okur-Chung Neurodevelopmental Syndrome (OCNDS) is caused by heterozygous mutations to the CSNK2A1 gene, which encodes the alpha subunit of casein kinase II (CK2). The most frequently occurring mutation is lysine 198 to arginine (K198R). To investigat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ab45f24cd08badd91743ca8712247fce
https://doi.org/10.1101/2021.04.05.438522
https://doi.org/10.1101/2021.04.05.438522
Autor:
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.
Publikováno v:
Frontiers in molecular biosciences [Front Mol Biosci] 2022 Apr 19; Vol. 9, pp. 850661. Date of Electronic Publication: 2022 Apr 19 (Print Publication: 2022).
