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

Garg, Divyani; Agarwal, Ayush; Faruq, Mohammed; Srivastava, Achal Kumar

Garg, Divyani; Agarwal, Ayush; Faruq, Mohammed; Srivastava, Achal Kumar.

Afiliación

Garg D; Department of Neurology, All India Institute of Medical Sciences, New Delhi, India.
Agarwal A; Department of Neurology, All India Institute of Medical Sciences, New Delhi, India.
Faruq M; Division of Genomics and Molecular Medicine, CSIR-Institute of Genomics and Integrative Biology (IGIB), New Delhi, India.
Srivastava AK; Department of Neurology, All India Institute of Medical Sciences, New Delhi, India.

J Mov Disord ; 17(2): 239-241, 2024 Apr.

Article en En | MEDLINE | ID: mdl-38419487

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Mov Disord Año: 2024 Tipo del documento: Article País de afiliación: India Pais de publicación: Corea del Sur

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