A rare cause of paroxysmal movement disorder associated with TBC1D24 Gene mutation in two siblings
Main Authors: | , |
---|---|
Format: | Article |
Language: | English |
Published: |
Wolters Kluwer Medknow Publications
2023-01-01
|
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 |
_version_ | 1797775338451763200 |
---|---|
author | Esra Sarıgecılı Ozlem Anlas |
author_facet | Esra Sarıgecılı Ozlem Anlas |
author_sort | Esra Sarıgecılı |
collection | DOAJ |
first_indexed | 2024-03-12T22:34:16Z |
format | Article |
id | doaj.art-1fa7a54ac0c549e89775f0faba71c51e |
institution | Directory Open Access Journal |
issn | 0972-2327 1998-3549 |
language | English |
last_indexed | 2024-03-12T22:34:16Z |
publishDate | 2023-01-01 |
publisher | Wolters Kluwer Medknow Publications |
record_format | Article |
series | Annals of Indian Academy of Neurology |
spelling | doaj.art-1fa7a54ac0c549e89775f0faba71c51e2023-07-21T14:20:16ZengWolters Kluwer Medknow PublicationsAnnals of Indian Academy of Neurology0972-23271998-35492023-01-0126329029310.4103/aian.aian_465_22A rare cause of paroxysmal movement disorder associated with TBC1D24 Gene mutation in two siblingsEsra SarıgecılıOzlem Anlashttp://www.annalsofian.org/article.asp?issn=0972-2327;year=2023;volume=26;issue=3;spage=290;epage=293;aulast=Sarıgecılı |
spellingShingle | Esra Sarıgecılı Ozlem Anlas A rare cause of paroxysmal movement disorder associated with TBC1D24 Gene mutation in two siblings Annals of Indian Academy of Neurology |
title | A rare cause of paroxysmal movement disorder associated with TBC1D24 Gene mutation in two siblings |
title_full | A rare cause of paroxysmal movement disorder associated with TBC1D24 Gene mutation in two siblings |
title_fullStr | A rare cause of paroxysmal movement disorder associated with TBC1D24 Gene mutation in two siblings |
title_full_unstemmed | A rare cause of paroxysmal movement disorder associated with TBC1D24 Gene mutation in two siblings |
title_short | A rare cause of paroxysmal movement disorder associated with TBC1D24 Gene mutation in two siblings |
title_sort | rare cause of paroxysmal movement disorder associated with tbc1d24 gene mutation in two siblings |
url | http://www.annalsofian.org/article.asp?issn=0972-2327;year=2023;volume=26;issue=3;spage=290;epage=293;aulast=Sarıgecılı |
work_keys_str_mv | AT esrasarıgecılı ararecauseofparoxysmalmovementdisorderassociatedwithtbc1d24genemutationintwosiblings AT ozlemanlas ararecauseofparoxysmalmovementdisorderassociatedwithtbc1d24genemutationintwosiblings AT esrasarıgecılı rarecauseofparoxysmalmovementdisorderassociatedwithtbc1d24genemutationintwosiblings AT ozlemanlas rarecauseofparoxysmalmovementdisorderassociatedwithtbc1d24genemutationintwosiblings |