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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.

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書目詳細資料
發表在:Pediatr Neurol Briefs
Main Authors: Chen, Wenjuan, Yuan, Hongjie
格式: Artigo
語言:Inglês
出版: Pediatric Neurology Briefs Publishers 2015
主題:
在線閱讀: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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