DFI is now a Platinum level GuideStar participant!
If you’ve never heard of GuideStar before, it’s a widely recognized company that gathers and reports information about every IRS-registered nonprofit organization, with the goal of encouraging charitable giving and helping potential donors make better decisions. Other companies and donors look to GuideStar to provide easily accessible info on 501(c)(3) charities…and DFI just completed the highest level of profile transparency available to achieve!
This means that if you know of anyone (employers, friends, or others looking to possibly donate) that might have any questions about our Foundation (our mission, legitimacy, impact, reputation, finances, programs, governance, etc.), you can direct them to GuideStar where they can review information on Deater Foundation Inc., and even donate right from there as well!
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The Gene Causing the Deater Disease Is Identified!
Important Research Results Published
Ellen Burns, Vice President and Medical Liaison
In the March 2001 edition, Volume 27, of the prestigious scientific journal Nature Genetics, two articles were published that were the culmination of years of research involving the Deater family and other families with a degenerative neurologic disease.
One article, Mutations in SPLTC1, encoding serine palmitoyltransferase, long chain base subunit-1, cause hereditary sensory neuropathy type I, was submitted by Jennifer Dawkins and her team at the Neurobiology Laboratory of University of Sydney, New South Wales, Australia, under the leadership of Garth Nicholson. For some years, now, this Australian group has been collaborating with the research group from the Day Neuromuscular Laboratory in Charlestown, Massachusetts to find the exact gene that causes the disease that affects the Deater family. This disease is known in medical circles as HSN I (Hereditary Sensory Neuropathy type I). In fact, some medical textbooks and research articles specifically refer to earlier published research on our family.
In the Nature Genetics article, the Australian researchers identify the specific gene, SPTLC1, on chromosome 9 (more specifically: 9q22.3), that is mutated, or different, in people who have HSN1. These researchers
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