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Missense variants in RPH3A cause defects in excitatory synaptic function and are associated with a clinically variable neurodevelopmental disorder.

Genetics in medicine : official journal of the American College of Medical Genetics | 2023

RPH3A encodes a protein involved in the stabilization of GluN2A subunit of N-methyl-D-aspartate (NMDA)-type glutamate receptors at the cell surface, forming a complex essential for synaptic plasticity and cognition. We investigated the effect of variants in RPH3A in patients with neurodevelopmental disorders.

Pubmed ID: 37403762 RIS Download

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Associated grants

  • Agency: NIMH NIH HHS, United States
    Id: U01 MH111661
  • Agency: NHGRI NIH HHS, United States
    Id: UM1 HG007301
  • Agency: Medical Research Council, United Kingdom
    Id: MR/S01165X/1
  • Agency: Medical Research Council, United Kingdom
    Id: MR/S005021/1
  • Agency: Medical Research Council, United Kingdom
    Id: G0601943
  • Agency: Medical Research Council, United Kingdom
    Id: MR/V012177/1
  • Agency: Department of Health, United Kingdom

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