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De Novo Mutations and Rare Variants Occurring in NMDA Receptors
A significant number of variants/mutations in the N-methyl-(D)-aspartate glutamatergic receptor (NMDAR) gene family (GRIN) have been identified along with stunning advances in the technologies of next generation of whole-exome sequencing. Mutations in human GRIN genes are distributed throughout the...
Tallennettuna:
| Julkaisussa: | Curr Opin Physiol |
|---|---|
| Päätekijät: | , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2017
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5945193/ https://ncbi.nlm.nih.gov/pubmed/29756080 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.cophys.2017.12.013 |
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