GRIN1 Mutations in Early-Onset Epileptic Encephalopathy
Investigators from Yokohama City University and other medical centers in Israel and Japan reported mutations on N-methyl-D-aspartate (NMDA) receptors subunit <em>GRIN1</em> (GluN1) identified in patients with nonsyndromic intellectual disability and early-onset epileptic encephalopathy.
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| Main Authors: | , |
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| Format: | Book |
| Published: |
Pediatric Neurology Briefs Publishers,
2015-06-01T00:00:00Z.
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| Subjects: | |
| Online Access: | Connect to this object online. |
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Internet
Connect to this object online.3rd Floor Main Library
| Call Number: |
A1234.567 |
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| Copy 1 | Available |