ReviewCerebellum (London, England)2018

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.

Mohammad A Al-Muhaizea et al.PubMed ↗Publisher ↗

No numbers read from the abstract.