Clinical and Genetic Characterization of Autosomal Recessive Spinocerebellar Ataxia Type 16 (SCAR16) in Taiwan.

In conclusion, SCAR16 is an important but often neglected diagnosis of cerebellar ataxia of unknown cause, and the isolated cerebellar ataxia without involvement of other systems cannot be a basis to exclude the possibility of STUB1-related disease. PMID: 32367277 [PubMed - as supplied by publisher]

https://www.ncbi.nlm.nih.gov/pubmed/32367277?dopt=Abstract

Source: Cerebellum - May 3, 2020 Category: Neuroscience Authors: Chiu HH, Hsaio CT, Tsai YS, Liao YC, Lee YC, Soong BW Tags: Cerebellum Source Type: research