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A Case of Chorea with Slow Saccades Caused by NKX2-1 Mutation.

Authors :
Vercammen J
Terryn J
Van Daele S
Vermeer S
Vandenberghe W
Source :
Movement disorders clinical practice [Mov Disord Clin Pract] 2024 Jun; Vol. 11 (6), pp. 738-741. Date of Electronic Publication: 2024 Mar 07.
Publication Year :
2024

Subjects

Subjects :
Humans
Nuclear Proteins genetics
Male
Female
Chorea genetics
Chorea physiopathology
Chorea diagnosis
Thyroid Nuclear Factor 1 genetics
Mutation
Saccades physiology
Saccades genetics
Transcription Factors genetics

Details

Language :
English
ISSN :
2330-1619
Volume :
11
Issue :
6
Database :
MEDLINE
Journal :
Movement disorders clinical practice
Publication Type :
Report
Accession number :
38454250
Full Text :
https://doi.org/10.1002/mdc3.14013
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