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A Rare Cause of Paroxysmal Movement Disorder Associated with TBC1D24 Gene Mutation in Two Siblings
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2023
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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 |
author_sort | Sarıgecılı, Esra |
collection | PubMed |
description | |
format | Online Article Text |
id | pubmed-10394464 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
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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