SHANK3 is the most prominent gene in autism patients. It has mutations that range from 1 to 2% among people who have autism spectrum disorders.

SHANK3 is a unique gene responsible for mediating the functions that take place within the postsynaptic densities in excitatory synapses.

Mice play an important role in the development of therapies for rare diseases like Phelan-McDermid Syndrome. These little guys make a big difference in getting us closer to a cure!

What is Phelan-McDermid Syndrome? What are its symptoms? How many people are affected? These are questions that caregivers of individuals with Phelan-McDermid Syndrome hear all of the time.

We are proud to be participating in Healx's webinar on the development of in vitro models for rare disease research on August 13, 2020.