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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:	Letters to the Editor
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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