The Synaptic Gene Study: Design and Methodology to Identify Neurocognitive Markers in Phelan-McDermid Syndrome and <i>NRXN1</i> Deletions.

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

Cooke, Jennifer; Molloy, Ciara J; Cáceres, Antonia San José; Dinneen, Thomas; Bourgeron, Thomas; Murphy, Declan; Gallagher, Louise; Loth, Eva.

Afiliação

Cooke J; Forensic and Neurodevelopmental Sciences, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, United Kingdom.
Molloy CJ; Department of Psychiatry, School of Medicine, Trinity College Dublin, Dublin, Ireland.
Cáceres ASJ; Forensic and Neurodevelopmental Sciences, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, United Kingdom.
Dinneen T; Fundación para la Investigación Biomédica del Hospital General Universitario Gregorio Marañón, Madrid, Spain.
Bourgeron T; Biomedical Research Networking Center for Mental Health Network (CIBERSAM), Madrid, Spain.
Murphy D; Department of Psychiatry, School of Medicine, Trinity College Dublin, Dublin, Ireland.
Gallagher L; Department of Neuroscience, Institut Pasteur, Paris, France.
Loth E; Forensic and Neurodevelopmental Sciences, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, United Kingdom.

Front Neurosci ; 16: 806990, 2022.

Article em En | MEDLINE | ID: mdl-35250452