Cerebellar ataxias: β‐III spectrin's interactions suggest common

Loss of β-III Spectrin Leads to Purkinje Cell Dysfunction

The three SCA5 mutations and -III spectrin expression.PCR analysis

Purkinje cell degeneration in Spnb3 −/− mice. (A) The molecular

Cerebellar ataxias: β‐III spectrin's interactions suggest common

The Classification of Autosomal Recessive Cerebellar Ataxias: a

Spectrin mutations cause spinocerebellar ataxia type 5

α-Synuclein Promotes Neuronal Dysfunction and Death by Disrupting

β-III-spectrin spinocerebellar ataxia type 5 mutation reveals a

βIII spectrin controls the planarity of Purkinje cell dendrites by

The Spread of Spectrin in Ataxia and Neurodegenerative Disease

PDF) Increased actin binding is a shared molecular consequence of

Protein-protein interaction networks in the spinocerebellar