Podcast

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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News

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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