New KIF1A Gene Mutation Linked to Rett, Ends One Girl’s 15-year Diagnostic Journey
Researchers have identified a new mutation in the KIF1A gene in a girl in Australia that is associated with Rett syndrome, ending her 15-year diagnostic journey. Two new other KIF1A mutations also were found in two patients showing a severe neurodevelopmental disorder with some Rett-like features. These mutations affected…