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Human GRIN2B variants in neurodevelopmental disorders
The development of whole exome/genome sequencing technologies has given rise to an unprecedented volume of data linking patient genomic variability to brain disorder phenotypes. A surprising number of variants have been found in the N-methyl-D-aspartate receptor (NMDAR) gene family, with the GRIN2B...
में बचाया:
| में प्रकाशित: | J Pharmacol Sci |
|---|---|
| मुख्य लेखकों: | , , , , |
| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
2016
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| विषय: | |
| ऑनलाइन पहुंच: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5125235/ https://ncbi.nlm.nih.gov/pubmed/27818011 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jphs.2016.10.002 |
| टैग : |
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