This website provides information on patients with mutations in the SHANK2 gene, including clinical data, molecular data, management and research options.

Mutations in the SHANK2 gene are associated with autism spectrum disorders (ASD).

This website was created to share and collect information about clinic, management and research projects to gather more knowledge and provide better treatment of patients with mutations in the SHANK2 gene.

Thomas Bourgeron, PI, Institut Pasteur, Paris, France, thomas.bourgeron@pasteur.fr

Richard Delorme, MD, PhD, APHP, Paris, France, richard.delorme@aphp.fr

Gudrun A. Rappold, MD, Institute of Human Genetics, University of Heidelberg, Heidelberg, Germany, gudrun_rappold@med.uni-heidelberg.de

Simone Berkel, MD, Institute of Human Genetics, University of Heidelberg, Heidelberg, Germany, Simone.Berkel@med.uni-heidelberg.de