A rare cause of paroxysmal movement disorder associated with TBC1D24 Gene mutation in two siblings
| Main Authors: | , |
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| Format: | Article |
| Language: | English |
| Published: |
Wolters Kluwer Medknow Publications
2023-01-01
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| Series: | Annals of Indian Academy of Neurology |
| Online Access: | http://www.annalsofian.org/article.asp?issn=0972-2327;year=2023;volume=26;issue=3;spage=290;epage=293;aulast=Sarıgecılı |