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 (SCI-Expanded, Scopus)