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

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

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PDF] Recessive Mutations in SPTBN2 Implicate β-III Spectrin in

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

βIII Spectrin Is Necessary for Formation of the Constricted Neck

Genetics of Dominant Ataxias

βIII spectrin controls the planarity of Purkinje cell dendrites by

Spectrins: molecular organizers and targets of neurological

Spinocerebellar ataxias (SCAs) caused by common mutations

Loss of β-III Spectrin Leads to Purkinje Cell Dysfunction

Spectrin mutations cause spinocerebellar ataxia type 5

Sodium channel levels and activity enhanced by β-III spectrin

Spinocerebellar ataxia Nature Reviews Disease Primers

Cerebellar ataxia and functional genomics: Identifying the routes

A human β-III-spectrin spinocerebellar ataxia type 5 mutation

Spectrins and human diseases - ScienceDirect

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