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Language deficits in GRIN2A mutations and Landau–Kleffner syndrome as neural dysrhythmias

2023-01-12

Abstract excerpt

<p>This paper examines epilepsy-related aphasias in connection with GRIN2A mutations, focusing on acquired childhood epileptic aphasias, in particular, on Landau-Kleffner syndrome (LKS). Characterizing LKS as neural dysrhythmias, we review how EEG abnormalities typically manifested during non-rapid eye movement (NREM) sleep as electrical status epilepticus are related to the sleeping disorders partly caused by GRI...

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Literature Corpus work
f53bf22b-023e-5546-9460-5a8004a543b0
DOI
10.31234/osf.io/q42z6
Open publication

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