The First Indian Patient With Benign Hereditary Chorea due to a De Novo Mutation in the NKX2-1 Gene
J Mov Disord
.
2024 Apr;17(2):239-241.
doi: 10.14802/jmd.23273.
Epub 2024 Feb 29.
Authors
Divyani Garg
1
,
Ayush Agarwal
1
,
Mohammed Faruq
2
,
Achal Kumar Srivastava
1
Affiliations
1
Department of Neurology, All India Institute of Medical Sciences, New Delhi, India.
2
Division of Genomics and Molecular Medicine, CSIR-Institute of Genomics and Integrative Biology (IGIB), New Delhi, India.
PMID:
38419487
PMCID:
PMC11082612
DOI:
10.14802/jmd.23273
No abstract available