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A Novel Homozygous Mutation in SPTBN2 Leads to Spinocerebellar Ataxia in a Consanguineous Family: Report of a New Infantile-Onset Case and Brief Review of the Literature

Crossref DOI link: https://doi.org/10.1007/s12311-017-0893-2

Published Online: 2017-12-01

Published Print: 2018-06

Update policy: https://doi.org/10.1007/springer_crossmark_policy

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