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Spinocerebellar ataxia 17: Inconsistency between phenotype and neuroimage findings
Jin Zhang1, Weihong Gu, Ying Hao
1Movement Disorder and Neurogenetics Research Center, China-Japan Friendship Hospital, Beijing, People's Republic China.
Annals of Indian Academy of Neurology
|December 17, 2013
Abstract:
Spinocerebellar ataxia 17 (SCA17) is an autosomal dominant neurodegenerative disease clinically characterized by the presence of cerebellar ataxia in combination with variable neurological symptoms. Here we report a Chinese SCA17 family which proband's clinical manifestation was inconsistent with the neuroimage findings.

