Eyelid myoclonic status epilepticus: A rare phenotype in spinal muscular atrophy with progressive myoclonic epilepsy associated with ASAH1 gene mutation


Akarsu E. O. , Tekturk P. , Yapici Z. , Tepgec F., Uyguner Z. O. , Baykan B.

SEIZURE-EUROPEAN JOURNAL OF EPILEPSY, vol.42, pp.49-51, 2016 (Journal Indexed in SCI) identifier identifier identifier

  • Publication Type: Article / Editorial Material
  • Volume: 42
  • Publication Date: 2016
  • Doi Number: 10.1016/j.seizure.2016.09.007
  • Title of Journal : SEIZURE-EUROPEAN JOURNAL OF EPILEPSY
  • Page Numbers: pp.49-51