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🌀GRIN2AC1845A / GluN2AN615K: modelling a severe childhood-onset epilepsy in rats to assess potential therapeutics
🏛University of Edinburgh (UK)
⏳Deadline: Friday, March 07, 2025
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About
In this PhD project the student will study the effects of a mutation that in humans causes a severe childhood-onset epilepsy (2) and results from the asparagine residue in the GluN2A subunit being replaced by a lysine residue – GluN2AN615K.
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علوم زیستی
پزشکی
https://www.findaphd.com/phds/project/grin2ac1845a-glun2an615k-modelling-a-severe-childhood-onset-epilepsy-in-rats-to-assess-potential-therapeutics/?p181889
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