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.
272906662
IČO
2010
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Georgetown, CT 06829 USA
Adresa
smsresearchfoundation.org
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SmithMagenisResearchFoundation
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Poslední komentáře

So inspired by the work SMSRF is doing! Understanding Smith-Magenis Syndrome is crucial, and I love how you're pushing for innovative treatments. Keep it up! ❤️
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Jennifer and Brian's story really touched my heart. Thank you for sharing the challenges and triumphs of raising Aaron. It helps us all understand and support families affected by SMS better! 🌟
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Poslední diskuze

What are some innovative treatment options currently being explored for Smith-Magenis Syndrome, and how can the community support these efforts?
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How can we enhance awareness and understanding of Smith-Magenis Syndrome among healthcare professionals and the general public?
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SMS Research Foundation
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O společnosti

- H20, G80 -

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.

Výzkum vrozených vad a genetických onemocnění Konkrétně pojmenované nemoci
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