Further corroboration of distinct functional features in SCN2A variants causing intellectual disability or epileptic phenotypes

Overview of attention for article published in Molecular Medicine, February 2019

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https://t.co/wgGb74AULg

01 Dec 2022

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LATEST ADDITIONS: Further corroboration of distinct functional features in SCN2A variants causing intellectual disability or epileptic phenotypes https://t.co/zOmKg85nIM

27 Jun 2022

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@lizmizerik This paper is pretty interesting, one of the missense is loss of function. Others are gains. No easy answers but at least you aren't crazy. https://t.co/Vj8W1tyVwf

17 Mar 2022

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RT @UZH_IPT: New publication alert! Check it out here: Further corroboration of distinct functional features in SCN2A variants causing inte…

12 Mar 2019

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