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A variant of Nesprin1 giant devoid of KASH domain underlies the molecular etiology of autosomal recessive cerebellar ataxia type I
Razafsky, David, Hodzic, DidierVolume:
78
Language:
english
Journal:
Neurobiology of Disease
DOI:
10.1016/j.nbd.2015.03.027
Date:
June, 2015
File:
PDF, 4.74 MB
english, 2015