Stxbp1 Foundation
Hospital & Health Care, 2001 Hamilton St, Philadelphia, Pennsylvania, 94597, United States, 1-10 Employees
Phone Number: +19*********
Who is STXBP1 FOUNDATION
The STXBP1 Foundation is a non-profit parent organization dedicated to ending STXBP1-related disorders. We are comprised of a diverse team of families and their supports, scientists and m...
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Headquarters: 2001 Hamilton St, Philadelphia, Pennsylvania, 94597, United States
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Date Founded: 2017
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Employees: 1-10
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Revenue: $50 Million to $100 Million
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Active Tech Stack: See technologies
Industry: Hospital & Health Care
SIC Code: 4225
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NAICS Code: 531130 |
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Frequently Asked Questions Regarding STXBP1 Foundation
Answer: STXBP1 Foundation's headquarters are located at 2001 Hamilton St, Philadelphia, Pennsylvania, 94597, United States
Answer: STXBP1 Foundation's phone number is +19*********
Answer: STXBP1 Foundation's official website is https://stxbp1disorders.org
Answer: STXBP1 Foundation's revenue is $50 Million to $100 Million
Answer: STXBP1 Foundation's SIC: 4225
Answer: STXBP1 Foundation's NAICS: 531130
Answer: STXBP1 Foundation has 1-10 employees
Answer: STXBP1 Foundation is in Hospital & Health Care
Answer: STXBP1 Foundation contact info: Phone number: +19********* Website: https://stxbp1disorders.org
Answer: The STXBP1 Foundation is a non-profit parent organization dedicated to ending STXBP1-related disorders. We are comprised of a diverse team of families and their supports, scientists and medical professionals. In fostering partnerships with physicians, researchers, and other foundations, we share learnings and efficiencies to increase awareness of this rare, genetic disorder and accelerate the time to finding a cure. We believe that through our work, we are leading the charge towards improved therapies and ultimately ending STXBP1-related disordesr. Our International STXBP1 Family has grown tremendously to 1000+ united and strong and we will only continue to grow our numbers as other families have access to genetic testing. Our Mission: -Create awareness in the disorders associated with STXBP1 mutations -Fund Research to accelerate discovery of a cure -Provide families with tools to help them understand the disease & how to get involved -Advocate to improve early detection -Foster activism to help change policies in favor of orphaned diseases -Improve the lives of our STXBP1 Family
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