The molecular mechanism of muscle dysfunction associated with the R133W mutation in Tpm2.2
Author:
Funder
Russian Science Foundation
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
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4. The primary causes of muscle dysfunction associated with the point mutations in Tpm3.12; conformational analysis of mutant proteins as a tool for classification of myopathies;Borovikov;Int. J. Mol. Sci.,2018
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