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A Rare Cause of Paroxysmal Movement Disorder Associated with TBC1D24 Gene Mutation in Two Siblings

Detalles Bibliográficos
Autores principales: Sarıgecılı, Esra, Anlas, Ozlem
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10394464/
https://www.ncbi.nlm.nih.gov/pubmed/37538433
http://dx.doi.org/10.4103/aian.aian_465_22
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author Sarıgecılı, Esra
Anlas, Ozlem
author_facet Sarıgecılı, Esra
Anlas, Ozlem
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spelling pubmed-103944642023-08-03 A Rare Cause of Paroxysmal Movement Disorder Associated with TBC1D24 Gene Mutation in Two Siblings Sarıgecılı, Esra Anlas, Ozlem Ann Indian Acad Neurol Letters to the Editor Wolters Kluwer - Medknow 2023 2023-04-24 /pmc/articles/PMC10394464/ /pubmed/37538433 http://dx.doi.org/10.4103/aian.aian_465_22 Text en Copyright: © 2023 Annals of Indian Academy of Neurology https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Letters to the Editor
Sarıgecılı, Esra
Anlas, Ozlem
A Rare Cause of Paroxysmal Movement Disorder Associated with TBC1D24 Gene Mutation in Two Siblings
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
topic Letters to the Editor
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10394464/
https://www.ncbi.nlm.nih.gov/pubmed/37538433
http://dx.doi.org/10.4103/aian.aian_465_22
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