SMS Research Foundation

Birth Defects, Genetic Diseases Research / Georgetown /

Smith-Magenis Syndrome Research Foundation

The mission of the Smith-Magenis Syndrome Research Foundation is to advance scientific research leading to innovative treatment options for people living with SMS. The mission of the SMS Research Foundation is to advance scientific research leading to innovative treatment options for people living with Smith-Magenis Syndrome (SMS). Since our founding in 2010, we have been singularly focused on investing in scientific research that will lead to life-changing therapeutics for this rare and complex genetic syndrome.
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272906662
EIN
2010
Founded
Georgetown, CT 06829 USA
Address
smsresearchfoundation.org
Web
SmithMagenisResearchFoundation
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News

02 čer
SMS Research Foundation

Have you gotten your ‘I Love Someone with SMS’ decal? This exclusive design is still available so you can proudly spread SMS awareness while supporting innovative research! 🔗 Get your decal today at smsresearchfoundation.org/sms-awareness-decals/ #SMS #researchishope #SMSRF #SMSResearchFoundation #SmithMagenisSyndrome (fb)

31 kvě
SMS Research Foundation

Strength and tenderness – together, they create an unstoppable force. This community is driven by both as we fight for individuals with SMS. 💜 #ShareMyStrengthSaturday #SMSRF #smithmagenissyndrome #SMS #smsresearchfoundation (fb)

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SMS Research Foundation
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About the organization

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Watch Now Aarons Story In the most loving and articulate way SMSRF board member Jennifer Sauer and her husband Brian open up about the challenges and complexities of raising their son Aaron with SmithMagenis Syndrome SMS. New Style Same Mission Introducing SMSRFs new visual identity designed to blend tradition with innovation. New SMS Research Findings Were excited to share the latest findings on the RAI1 gene pivotal in brain development explored through innovative studies in mice marmosets and human cells. Exciting News.

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