Cerebellar ataxias: β‐III spectrin's interactions suggest common
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Clinical and functional characterization of a novel STUB1
Novel genes bearing mutations in rare cases of early-onset ataxia
Spinocerebellar ataxias (SCAs) caused by common mutations
PDF] Recessive Mutations in SPTBN2 Implicate β-III Spectrin in
A Protein–Protein Interaction Network for Human Inherited Ataxias
A human β-III-spectrin spinocerebellar ataxia type 5 mutation
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βIII spectrin controls the planarity of Purkinje cell dendrites by
Autosomal Recessive Cerebellar Ataxias: Paving the Way toward
βIII Spectrin Is Necessary for Formation of the Constricted Neck
PDF] Recessive Mutations in SPTBN2 Implicate β-III Spectrin in
