Welcome to the EEF1A2 Patient Insights Network

  

Join patients around the world in building the PIN community.

START MY PROFILE

  

Find out about research studies and clinical trials.

LEARN MORE

  

Advance research and speed development of new treatments.

SHARE

T
he EEF1A2 International Patient Insights Network (PIN) is designed to create a central registry for information on patients with mutations in EEF1A2. The more information we can compile with more consistency, the better our chances of understanding how mutations in EEF1A2 cause epilepsy and intellectual disability. 
 
With this PIN, we will be able to track outcomes, pull together information on treatment effectiveness, and ultimately, design better therapeutic strategies, including the development of new drugs.
Frontpage Slideshow | Copyright © 2006-2011 JoomlaWorks Ltd.

Click here to register now!

T
he EEF1A2 International Patient Insights Network (PIN) is designed to create a central registry for information on patients with mutations in EEF1A2. The more information we can compile with more consistency, the better our chances of understanding how mutations in EEF1A2 cause epilepsy and intellectual disability. 
 
With this PIN, we will be able to track outcomes, pull together information on treatment effectiveness, and ultimately, design better therapeutic strategies, including the development of new drugs.

Phones and tablets may default the first letter to uppercase.

LEARN MORE