An Overview of SCN2A

Prof Ingrid Scheffer has published many key papers in SCN2A and genetic epilepsies and discusses the progress that has been made in understanding SCN2A.

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Natural History Study in SCN2A

The SCN2A International Natural History Study (NHS) is comprised of clinicians collaborating from multiple academic institutions, including US, European and Australian based clinicians. Dr. Katherine

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REMINDER: TOMORROW @ 11am AESTSCN2A NATURAL HISTORY STUDY - UPDATESIGN UP HERE: us02web.zoom.us/meeting/register/tZAuce-hrzMrGddJHfV3XptHABnHz5sJj3QM ... See MoreSee Less
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Join us on Sunday at the Global Genes regional meeting. It starts at 7pm with presentations from around our region. SCN2A Highlights and relevant presentations -SCN2A Family Story - Ursula DelaneySCN2A Panelist - Kris PierceSCN2A Natural History Study Poster - International Team Genetic Epilepsy and Supporting Families- Dr Emma PalmerUNdiagnosed and Rare - Heather Renton - CEO, Syndromes Without A Name - SWAN AustraliaIf you register for the regional meeting you get access to the full @global genes summit. All presentations will be available for 6 months post the conference.globalgenes.org/event/rare-patient-advocacy-summit/Message me for the regional code to join for FREE.#SCN2A #gg2021 #raredisease #CureSCN2A ... See MoreSee Less
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