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

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

Clinical and functional characterization of a novel STUB1

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Genetics of Dominant Ataxias

Ankyrin-R Links Kv3.3 to the Spectrin Cytoskeleton and Is Required

The role of spectrin in cell adhesion and cell–cell contact

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

Polyglutamine spinocerebellar ataxias — from genes to potential

The Classification of Autosomal Recessive Cerebellar Ataxias: a

Spectrin mutations cause spinocerebellar ataxia type 5