Molecular mechanism of Spinocerebellar Ataxia type 6: glutamine repeat disorder, channelopathy and transcriptional dysregulation. The multifaceted aspects of a single mutation-Reference-Cited by-同舟云学术

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

Published:2015-02-16 Issue: Volume:9 Page:
ISSN:1662-5102
Container-title:Frontiers in Cellular Neuroscience
language:
Short-container-title:Front. Cell. Neurosci.

Author:

Giunti Paola,Mantuano Elide,Frontali Marina,Veneziano Liana

Publisher

Frontiers Media SA

Subject

Cellular and Molecular Neuroscience

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