Spinocerebellar Ataxia Type 4: A Novel Polyglycine Disease Caused by GGC Repeat Expansion in ZFHX3

Discover how Dr. Stefan Pulst used a novel genome sequencing technique to shed new light on a surprisingly complex mutation that causes a unique phenotype of ataxia. This highlighted research was presented during the 2024 International Congress of Parkinson’s Disease and Movement Disorders (mdscongress.org). Authors: S. Pulst (Salt Lake City, USA). Read the full abstract at mdsabstracts.org.