Molecular mechanism of Spinocerebellar Ataxia type 6: glutamine repeat disorder, channelopathy and transcriptional dysregulation. The multifaceted aspects of a single mutation

Overview of attention for article published in Frontiers in Cellular Neuroscience, February 2015

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Nerded out over this paper yesterday. What an amazing story!! https://t.co/qomdchnJCV

Molecular mechanism of Spinocerebellar Ataxia type 6: glutamine repeat disorder, channelopathy and transcriptional… http://t.co/7CfFn8UecA

Molecular mechanism of Spinocerebellar Ataxia type 6: glutamine repeat disorder, channelopathy and transcriptional… http://t.co/7CfFn8UecA

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