Supplemental material
Journal of Biomolecular Structure and Dynamics
Volume 36, 2018 - Issue 4
Research Articles
The proteinopathy of D169G and K263E mutants at the RNA Recognition Motif (RRM) domain of tar DNA-binding protein (tdp43) causing neurological disorders: A computational study
Vishwambhar Vishnu BhandareCentre for Bioinformatics, Pondicherry University, Pondicherry605014, India
http://orcid.org/0000-0001-8289-1959
http://orcid.org/0000-0001-8289-1959 & Amutha RamaswamyCentre for Bioinformatics, Pondicherry University, Pondicherry605014, IndiaCorrespondence[email protected]
http://orcid.org/0000-0002-4677-2263
http://orcid.org/0000-0002-4677-2263Reprints and Corporate Permissions
Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?
To request a reprint or corporate permissions for this article, please click on the relevant link below:
Academic Permissions
Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?
Obtain permissions instantly via Rightslink by clicking on the button below:
If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.
Related Research Data
The proteinopathy of D169G and K263E mutants at the RNA Recognition Motif (RRM) domain of tar DNA-binding protein (tdp43) causing neurological disorders: A computational study.
Source:
Taylor & Francis
Linking provided by
