Research identifies NKX2-1 downstream regulatory structural variants as significant contributors to molecular diagnoses in benign hereditary chorea. This discovery enhances understanding of the genetic underpinnings of the disease.
nkx2 1 downstream regulatory structural variants explain a substantial proportion of molecular diagnoses in patients with benign hereditary chorea
Original title: “NKX2-1 Downstream Regulatory Structural Variants Explain a Substantial Proportion of Molecular Diagnoses in Patients With Benign Hereditary Chorea.”