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Article

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

Seizure - 1 Nov 2016

Oguz Akarsu Emel, Tekturk Pınar, Yapici Zuhal, Tepgec Fatih, Uyguner Z Oya, Baykan Betul

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 27723502
DOI: 10.1016/j.seizure.2016.09.007

Genes

ASAH1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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