Structure of the MeCP2–TBLR1 complex reveals a molecular basis for Rett syndrome and related disorders
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Title
Structure of the MeCP2–TBLR1 complex reveals a molecular basis for Rett syndrome and related disorders
Authors
Keywords
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Journal
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
Volume 114, Issue 16, Pages E3243-E3250
Publisher
Proceedings of the National Academy of Sciences
Online
2017-03-28
DOI
10.1073/pnas.1700731114
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Note: Only part of the references are listed.- Integrating population variation and protein structural analysis to improve clinical interpretation of missense variation: application to the WD40 domain
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- (2013) Matthew J Lyst et al. NATURE NEUROSCIENCE
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- PHENIX: a comprehensive Python-based system for macromolecular structure solution
- (2010) Paul D. Adams et al. ACTA CRYSTALLOGRAPHICA SECTION D-BIOLOGICAL CRYSTALLOGRAPHY
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