Beta-III spectrin mutation L253P associated with spinocerebellar ataxia type 5 interferes with binding to Arp1 and protein trafficking from the Golgi. (Q34083706)

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English	Beta-III spectrin mutation L253P associated with spinocerebellar ataxia type 5 interferes with binding to Arp1 and protein trafficking from the Golgi.	scientific article

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7 February 2020

Beta-III spectrin mutation L253P associated with spinocerebellar ataxia type 5 interferes with binding to Arp1 and protein trafficking from the Golgi (English)

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7 February 2020

spinocerebellar ataxia type 5

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Alastair R. Lyndon

4

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7 February 2020

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Yvonne L Clarkson

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7 February 2020

Trudi Gillespie

2

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7 February 2020

Emma M Perkins

3

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7 February 2020

Mandy Jackson

5

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7 February 2020

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5 July 2010

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7 February 2020

Human Molecular Genetics

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7 February 2020

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7 February 2020

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7 February 2020

3634-3641

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7 February 2020

Loss of beta-III spectrin leads to Purkinje cell dysfunction recapitulating the behavior and neuropathology of spinocerebellar ataxia type 5 in humans.

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10.1093/HMG/DDQ279

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7 February 2020

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7 February 2020

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