J Mov Disord.
2024 Apr;17(2):239-241. 10.14802/jmd.23273.
The First Indian Patient With Benign Hereditary Chorea due to a De Novo Mutation in the NKX2-1 Gene
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- 1Department of Neurology, All India Institute of Medical Sciences, New Delhi, India
- 2Division of Genomics and Molecular Medicine, CSIR-Institute of Genomics and Integrative Biology (IGIB), New Delhi, India
- KMID: 2554704
- DOI: http://doi.org/10.14802/jmd.23273
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