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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 GRIN1 (GluN1) identified in patients with nonsyndromic intellectual disability and early-onset epileptic encephalopathy.
Tallennettuna:
| Julkaisussa: | Pediatr Neurol Briefs |
|---|---|
| Päätekijät: | , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Pediatric Neurology Briefs Publishers
2015
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4747309/ https://ncbi.nlm.nih.gov/pubmed/26933583 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.15844/pedneurbriefs-29-6-3 |
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