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


Akarsu E., Tekturk P., YAPICI Z., Tepgec F., UYGUNER Z. O., BAYKAL B.

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