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- W2321817991 abstract "A spate of human genetic studies has identified mutations in NMDAR subunits as a root cause of idiopathic focal epilepsy, a common childhood form of the disease. The studies suggest that a group of epilepsies and encephalopathies marked by seizures, aphasia and learning disorders could be treated with NMDAR-selective modulators." @default.
- W2321817991 created "2016-06-24" @default.
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- W2321817991 date "2013-09-01" @default.
- W2321817991 modified "2023-10-16" @default.
- W2321817991 title "Epilepsy narrows down" @default.
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- W2321817991 doi "https://doi.org/10.1038/scibx.2013.916" @default.
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