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SCN2A- The FamilieSCN2A Foundation

Scn2 A The Familie Scn2 A Foundation

Research, P.O. Box 82, East Longmeadow, , 1028, Massachusetts, United States, 1-10 Employees

scn2a.org

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phone no Phone Number: +16*********

Who is SCN2A- THE FAMILIESCN2A FOUNDATION

We are an organization created by parents of children diagnosed with rare forms of Epilepsy and Autism as a result of a change in the SCN2A gene. Our vision is to find effective treatment...

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  • P.O. Box 82, East Longmeadow, Massachusetts, 1028, United States Headquarters: P.O. Box 82, East Longmeadow, Massachusetts, 1028, United States
  • 2014 Date Founded: 2014
  • 1-10 Employees: 1-10
  • dollar-icon Revenue: $1 Billion and Over
  • tech-icon Active Tech Stack: See technologies

industries-icon Industry: Research

SIC SIC Code: 8092 | NAICS Code: 621492 | Show More

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SCN2A- The FamilieSCN2A Foundation Org Chart and Mapping

Employees
Leah Myers

Leah Myers

Executive Director

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Frequently Asked Questions Regarding SCN2A- The FamilieSCN2A Foundation

Answer: SCN2A- The FamilieSCN2A Foundation's headquarters are located at P.O. Box 82, East Longmeadow, , 1028, Massachusetts, United States

Answer: SCN2A- The FamilieSCN2A Foundation's phone number is +16*********

Answer: SCN2A- The FamilieSCN2A Foundation's official website is https://scn2a.org

Answer: SCN2A- The FamilieSCN2A Foundation's revenue is $1 Billion and Over

Answer: SCN2A- The FamilieSCN2A Foundation's SIC: 8092

Answer: SCN2A- The FamilieSCN2A Foundation's NAICS: 621492

Answer: SCN2A- The FamilieSCN2A Foundation has 1-10 employees

Answer: SCN2A- The FamilieSCN2A Foundation is in Research

Answer: SCN2A- The FamilieSCN2A Foundation contact info: Phone number: +16********* Website: https://scn2a.org

Answer: We are an organization created by parents of children diagnosed with rare forms of Epilepsy and Autism as a result of a change in the SCN2A gene. Our vision is to find effective treatments and a cure for SCN2A related disorders. Our mission is to improve the lives of those affected by SCN2A related disorders through research, public awareness, family support and patient advocacy. We are a registered 501(c)(3) organization.

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