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The Synaptic Gene Study: Design and Methodology to Identify Neurocognitive Markers in Phelan-McDermid Syndrome and NRXN1 Deletions. (2022)

First Author: Cooke J

Attributed to: MRC Centre for Neurodevelopmental Disorders funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.3389/fnins.2022.806990

PubMed Identifier: 35250452

Publication URI: http://europepmc.org/abstract/MED/35250452

Type: Journal Article/Review

Volume: 16

Parent Publication: Frontiers in neuroscience

ISSN: 1662-453X