Annals of Indian Academy of Neurology (Jan 2023)

A rare cause of paroxysmal movement disorder associated with TBC1D24 Gene mutation in two siblings

  • Esra Sarıgecılı,
  • Ozlem Anlas

DOI
https://doi.org/10.4103/aian.aian_465_22
Journal volume & issue
Vol. 26, no. 3
pp. 290 – 293

Abstract

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