Biallelic ELMO3 mutations and loss of function for DOCK-mediated RAC1 activation result in intellectual disability

Author:

Tran Viviane12,Goyette Marie-Anne13,Martínez-García Mónica4,Jiménez de Domingo Ana5,Fernández-Mayoralas Daniel Martín5,Fernández-Perrone Ana Laura5,Tirado Pilar6,Calleja-Pérez Beatriz7,Álvarez Sara4,Côté Jean-François1238ORCID,Fernández-Jaén Alberto59

Affiliation:

1. Laboratory of Cytoskeletal Organization and Cell Migration, Montreal Clinical Research Institute (IRCM), Montréal, QC, Canada

2. Department of Biochemistry and Molecular Medicine, Université De Montréal, Montréal, QC, Canada

3. Molecular Biology Programs, Université De Montréal, Montréal, QC, Canada

4. Department of Genomics and Medicine, NIMGenetics, Madrid, Spain

5. Department of Pediatric Neurology. ónsalud. Madrid. Spain

6. Department of Pediatric Neurology. Hospital Universitario La Paz. Madrid. Spain

7. Pediatric Primary Care. C. S. Doctor Cirajas. Madrid. Spain

8. Department of Anatomy and Cell Biology, McGill University, Montréal, QC, Canada

9. Department of Pediatric Neurology, Medicine School. Universidad Europea De, Madrid, Spain

Funder

Cancer Research

CIHR

Publisher

Informa UK Limited

Subject

Cell Biology,Biochemistry

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