- The First Indian Patient With Benign Hereditary Chorea due to a De Novo Mutation in the NKX2-1 Gene
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Divyani Garg, Ayush Agarwal, Mohammed Faruq, Achal Kumar Srivastava
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J Mov Disord. 2024;17(2):239-241. Published online February 29, 2024
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DOI: https://doi.org/10.14802/jmd.23273
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