Biallelic inherited SCN8A variants, a rare cause of SCN8A-related developmental and epileptic encephalopathy

Eric R. Wengert, Cathrine E. Tronhjem, Jacy L. Wagnon, Katrine M. Johannesen, Hayley Petit, Ilona Krey, Anusha U. Saga, Payal S. Panchal, Samantha M. Strohm, Jörn Lange, Susanne B. Kamphausen, Guido Rubboli, Johannes R. Lemke, Elena Gardella, Manoj K. Patel, Miriam H. Meisler*, Rikke S. Møller

*Kontaktforfatter

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

51 Downloads (Pure)

Fingeraftryk

Dyk ned i forskningsemnerne om 'Biallelic inherited SCN8A variants, a rare cause of SCN8A-related developmental and epileptic encephalopathy'. Sammen danner de et unikt fingeraftryk.

Biochemistry, Genetics and Molecular Biology