Skip to main navigation Skip to search Skip to main content

De novo SCN1A mutations are a major cause of severe myoclonic epilepsy of infancy

Lieve Claes, Berten Ceulemans, Dominique Audenaert, Katrien Smets, Ann Löfgren, Jurgen Del-Favero, Sirpa Ala-Mello, Lina Basel-Vanagaite, Barbara Plecko, Salmo Raskin, Paul Thiry, Nicole I Wolf, Christine Van Broeckhoven, Peter De Jonghe

Research output: Contribution to journal › Article › peer-review

175 Citations (Scopus)

Fingerprint

Dive into the research topics of 'De novo SCN1A mutations are a major cause of severe myoclonic epilepsy of infancy'. Together they form a unique fingerprint.
Sort by

Neuroscience