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

IF 2.5 4区 医学 Q2 CLINICAL NEUROLOGY
Journal of Movement Disorders Pub Date : 2024-04-01 Epub Date: 2024-02-29 DOI:10.14802/jmd.23273
Divyani Garg, Ayush Agarwal, Mohammed Faruq, Achal Kumar Srivastava
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首例因 NKX2-1 基因新突变而导致良性遗传性舞蹈症的印度患者。
本文章由计算机程序翻译，如有差异，请以英文原文为准。
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来源期刊
Journal of Movement Disorders
Journal of Movement Disorders CLINICAL NEUROLOGY-
CiteScore
2.50
自引率
5.10%
发文量
49
审稿时长
12 weeks
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