Published 2015
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GRIN1 Mutations in Early-Onset Epileptic Encephalopathy
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Abstract
Investigators from Yokohama City University and other medical centers in Israel and Japan reported mutations on N-methyl-D-aspartate (NMDA) receptors subunit GRIN1 (GluN1) identified in patients with nonsyndromic intellectual disability and early-onset epileptic encephalopathy.Files
PNB-29-44.pdf
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- PNB-29-44
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2015When the item was originally created.