Movement disorder phenotype in CTNNB1-syndrome: A complex but recognizable phenomenology
Parkinsonism Relat Disord. 2024 Jul 9;126:107057. doi: 10.1016/j.parkreldis.2024.107057. Online ahead of print. ABSTRACT INTRODUCTION: CTNNB1 gene loss-of-function variants cause Neurodevelopmental disorder with spastic diplegia and …