The First Indian Patient With Benign Hereditary Chorea due to a De Novo Mutation in the NKX2-1 Gene
- Author:
Divyani GARG
1
;
Ayush AGARWAL
;
Mohammed FARUQ
;
Achal Kumar SRIVASTAVA
Author Information
- Publication Type:10
- From:Journal of Movement Disorders 2024;17(2):239-241
- CountryRepublic of Korea
- Language:EN
