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pro vyhledávání: '"Nhat Q, Phan"'
Autor:
Danielle M. Caefer, Nhat Q. Phan, Jennifer C. Liddle, Jeremy L. Balsbaugh, Joseph P. O’Shea, Anastasios V. Tzingounis, Daniel Schwartz
Publikováno v:
Frontiers in Molecular Biosciences, Vol 9 (2022)
Okur-Chung Neurodevelopmental Syndrome (OCNDS) is caused by heterozygous mutations to the CSNK2A1 gene, which encodes the alpha subunit of protein kinase CK2. The most frequently occurring mutation is lysine 198 to arginine (K198R). To investigate th
Externí odkaz:
https://doaj.org/article/48a3629b5e9c48248660445d518f72c2
