Editorial: Deciphering the etiology of rare genetic disorders associated with protein phosphatases

Front Cell Dev Biol. 2023 Aug 14:11:1241606. doi: 10.3389/fcell.2023.1241606. eCollection 2023.

Veerle Janssens^{1

2

3}, Brian E Wadzinski⁴, Chenchen Li⁵, Richard E Honkanen⁵

¹ Laboratory of Protein Phosphorylation and Proteomics, Department of Cellular and Molecular Medicine, University of Leuven (KU Leuven), Leuven, Belgium.
² KU Leuven Brain Institute (LBI), Leuven, Belgium.
³ KU Leuven Cancer Institute (LKI), Leuven, Belgium.
⁴ Department of Pharmacology, Vanderbilt University School of Medicine, Nashville, TN, United States.
⁵ Department of Biochemistry and Molecular Biology, University of South Alabama, Mobile, AL, United States.

No abstract available

Keywords: PPP2CA; PPP2R5D; PTPN11; de novo variant; developmental disorder; genetic disorder; protein phosphatase (PP); signal transduction.

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