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pro vyhledávání: '"Pankaj S. Parihar"'
Autor:
Cheng-Guo Wu, Vijaya K. Balakrishnan, Pankaj S. Parihar, Kirill Konovolov, Yu-Chia Chen, Ronald A Merrill, Hui Wei, Bridget Carragher, Ramya Sundaresan, Qiang Cui, Brian E. Wadzinski, Mark R. Swingle, Alla Musiyenko, Richard Honkanen, Wendy K. Chung, Aussie Suzuki, Stefan Strack, Xuhui Huang, Yongna Xing
An increasing number of mutations associated with devastating human diseases are diagnosed by whole-genome/exon sequencing. Recurrentde novomissense mutations have been discovered in B56δ (encoded byPPP2R5D), a regulatory subunit of protein phosphat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e8c7723ac5bfc49c8706fa023d5ad09e
https://doi.org/10.1101/2023.03.09.530109
https://doi.org/10.1101/2023.03.09.530109