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All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year Sort by creator [A → Z]' creator [Z → A]' publishing year ↑ (asc)' publishing year ↓ (desc)' title [A → Z]' title [Z → A]' Simple Search Hits 1 – 2 of 2 1 Update on the genetics of the epilepsy-aphasia spectrum and role of GRIN2A mutations Lesca, Gaëtan; Moller, Rikke S.; Rudolf, Gabrielle... In: ISSN: 1294-9361 ; Epileptic Disorders ; https://hal.archives-ouvertes.fr/hal-02350836 ; Epileptic Disorders, John Libbey Eurotext, 2019, ⟨10.1684/epd.2019.1056⟩ (2019) BASE Show details 2 Delineating the GRIN1 phenotypic spectrum: a distinct genetic NMDA receptor encephalopathy Lemke, Johannes R.; Geider, Kirsten; Helbig, Katherine L.. - : Lippincott, Williams & Wilkins, 2016 BASE Show details

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