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Title
Mechanism for autoinhibition and activation of the MORC3 ATPase
Authors
Keywords
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Journal
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
Volume 116, Issue 13, Pages 6111-6119
Publisher
Proceedings of the National Academy of Sciences
Online
2019-03-09
DOI
10.1073/pnas.1819524116
References
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- (2016) Gaurav Jadhav et al. Scientific Reports
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- (2012) Susanne A.I. Seidel et al. METHODS
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