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

Internet

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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