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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 GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction Lesca, G; Rudolf, G; Bruneau, N... In: Symplectic Elements at Oxford ; Scopus (http://www.scopus.com/home.url) (2013) BASE Show details 2 Severe neonatal episodic laryngospasm due to de novo SCN4A mutations: a new treatable disorder. Lion-Francois, L.; Mignot, C.; Vicart, S.... In: ISSN: 0028-3878 ; EISSN: 1526-632X ; Neurology ; https://hal.archives-ouvertes.fr/hal-00655293 ; Neurology, American Academy of Neurology, 2010, 75 (7), pp.641-5. ⟨10.1212/WNL.0b013e3181ed9e96⟩ (2010) BASE Show details

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