Welcome to the EEF1A2 Patient Insights Network

  

Join patients around the world in building the PIN community.

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Find out about research studies and clinical trials.

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Advance research and speed development of new treatments.

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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.

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.

LEARN MORE