Media type: E-Article Title: Deep phenotyping reveals patients with SYNGAP1 mutations have a multi-domain neurological disorder (5087) Contributor: Holder, Jimmy; Lyons-Warren, Ariel; Risen, Sarah; Stowe, Robert; mccormack, maria; Vinson, Sherry; Bolbocean, Corneliu; Smith-Hicks, Constance imprint: Ovid Technologies (Wolters Kluwer Health), 2021 Published in: Neurology Language: English DOI: 10.1212/wnl.96.15_supplement.5087 ISSN: 0028-3878; 1526-632X Keywords: Neurology (clinical) Origination: Footnote: