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You searched for: Author/Creator Myers, Scott J.

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1. A novel missense mutation in GRIN2A causes a nonepileptic neurodevelopmental disorder. Issue 6 (11th April 2018)

2. Compound‐heterozygous GRIN2A null variants associated with severe developmental and epileptic encephalopathy. Issue 10 (30th August 2022)

3. Hodgkin–Huxley–Katz Prize Lecture: Genetic and pharmacological control of glutamate receptor channel through a highly conserved gating motif. (15th June 2020)

4. Negative allosteric modulation of GluN1/GluN3 NMDA receptors. (1st October 2020)

5. The GRIA3 c.2477G > A Variant Causes an Exaggerated Startle Reflex, Chorea, and Multifocal Myoclonus. Issue 7 (5th May 2020)