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Missense variants in RPH3A cause defects in excitatory synaptic function and are associated with a clinically variable neurodevelopmental disorder (2023)

First Author: Lisa Pavinato

Attributed to: MRC Strategic Award to establish an International Centre for Genomic Medicine in Neuromuscular Diseases funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.60692/dvz5j-5hn06

Publication URI: https://gresis.osc.int//doi/10.60692/dvz5j-5hn06

Type: Other