Face-valid phenotypes in a mouse model of the most common mutation in EEF1A2-related neurodevelopmental disorder

• Grant F. Marshall,
• Melissa Fasol,
• Faith C. J. Davies,
• Matthew Le Seelleur,
• Alejandra Fernandez Alvarez,
• Cavan Bennett-Ness,
• Alfredo Gonzalez-Sulser,
• Catherine M. Abbott

Affiliations

Grant F. Marshall

Centre for Genomic & Experimental Medicine, MRC Institute of Genetics and Molecular Medicine, University of Edinburgh, Western General Hospital, Crewe Road, Edinburgh EH4 2XU, UK

Melissa Fasol

Simons Initiative for the Developing Brain, University of Edinburgh, Edinburgh EH8 9XD, UK

Faith C. J. Davies

Centre for Genomic & Experimental Medicine, MRC Institute of Genetics and Molecular Medicine, University of Edinburgh, Western General Hospital, Crewe Road, Edinburgh EH4 2XU, UK

Matthew Le Seelleur

Centre for Genomic & Experimental Medicine, MRC Institute of Genetics and Molecular Medicine, University of Edinburgh, Western General Hospital, Crewe Road, Edinburgh EH4 2XU, UK

Alejandra Fernandez Alvarez

Centre for Genomic & Experimental Medicine, MRC Institute of Genetics and Molecular Medicine, University of Edinburgh, Western General Hospital, Crewe Road, Edinburgh EH4 2XU, UK

Cavan Bennett-Ness

Centre for Genomic & Experimental Medicine, MRC Institute of Genetics and Molecular Medicine, University of Edinburgh, Western General Hospital, Crewe Road, Edinburgh EH4 2XU, UK

Alfredo Gonzalez-Sulser

Simons Initiative for the Developing Brain, University of Edinburgh, Edinburgh EH8 9XD, UK

Catherine M. Abbott

Centre for Genomic & Experimental Medicine, MRC Institute of Genetics and Molecular Medicine, University of Edinburgh, Western General Hospital, Crewe Road, Edinburgh EH4 2XU, UK