A variant of Nesprin1 giant devoid of KASH domain underlies the molecular etiology of autosomal recessive cerebellar ataxia type I

Title
A variant of Nesprin1 giant devoid of KASH domain underlies the molecular etiology of autosomal recessive cerebellar ataxia type I
Authors
Keywords
ARCA1, Autosomal recessive cerebellar ataxia Type I, Cerebellar granule neuron, Cerebellar mossy fiber, Cerebellum, KASH, KLNes1g, Nesprin, Spinocerebellar ataxia
Journal
NEUROBIOLOGY OF DISEASE
Volume 78, Issue -, Pages 57-67
Publisher
Elsevier BV
Online
2015-04-06
DOI
10.1016/j.nbd.2015.03.027

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