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SCA19

Newly identified mutations in SCA19/22 and their dysfunctions

Written by Sophia Leung Edited by Dr. Marija Cvetanovic While the mutant proteins in SCA19/22 lose part of their innate functions and properties, they also disrupt the key functions of the normal healthy protein. The underlying mechanism of the hereditary property of SCA19/22 is elusive. In this study, the researchers Read More…

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