The discovery of the mutation in the SHANK3 gene, responsible for about one million cases of autism worldwide, could lead to ...

The FDA designation marks a significant milestone in the development of a novel treatment for a rare neurodevelopmental disorderPlan to initiate ...

In contrast, Shank3 mutant dogs displayed deficits in face categorization. This study provides direct experimental evidence that mutations in Shank3 lead to ASD-like deficits in face processing ...

New research has uncovered a disrupted brain communication pathway in children with autism that impairs their ability to quickly shift attention—an essential skill for social interaction.

PMS is a rare genetic disorder most commonly caused by deletions or mutations affecting the SHANK3 gene leading to a range of symptoms, including global developmental delay, intellectual ...