The First Indian Patient With Benign Hereditary Chorea due to a De Novo Mutation in the NKX2-1 Gene

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Bibliographic Details
Published in:Journal of movement disorders 2024-04, Vol.17 (2), p.239-241
Main Authors: Garg, Divyani, Agarwal, Ayush, Faruq, Mohammed, Srivastava, Achal Kumar
Format: Article
Language:English
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ISSN:2005-940X
2093-4939
DOI:10.14802/jmd.23273