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