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GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction
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In: Symplectic Elements at Oxford ; Scopus (http://www.scopus.com/home.url) (2013)
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Severe neonatal episodic laryngospasm due to de novo SCN4A mutations: a new treatable disorder.
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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)
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