C12orf65 gene, a rare form of CMT also known as Leigh Syndrome is robbing young children of a normal life even beyond the classic CMT symptoms.
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Research
Total posts in Category: 98
Won’t You Please Consider A Year End Gift?
Learn the top 15 ways the Hereditary Neuropathy Foundation put your generous donations to work for you this year.
PNS, It’s A Global Effort
Where do the top CMT researchers in the world unite to share leading-edge research? The Peripheral Nerve Society (PNS) meeting!
HNF & Inspire Present Poster at Global Genes 2019 Rare Drug Development Symposium
In 2009, HNF partnered with Inspire, a social network for health, to launch a CMT online support community.
HNF Presents Research Findings at Three Prestigious Conferences
Read more about the research findings presented at these conferences.
HNF is Now Recruiting Patients for New Gene Therapy Research Projects
HNF has selected its first three types of CMT based on their potential for success…and we need your help!
Orphan Disease Center Million Dollar Bike Ride Pilot Grant Program
The ODC MDBR Pilot Grant Program provides a one‐year grant to support research related to a rare disease represented in the 2019 Million Dollar Bike Ride.
What Is Fast Track?
The FDA has awarded Fast Track designation to two drugs currently in development for CMT.
HNF Featured in Rare Neurological Disease Special Report
HNF is proud to announce that for the fifth year in a row, we have been featured in the annual Rare Neurological Disease Special Report.
StarWise Therapeutics & HNF Form A Strategic Alliance to Bring a NextGen HDAC6 Drug Therapy to CMT2A (MFN2) Patients
HNF has been committed to funding HDAC inhibitor research since 2014.
CMT On The Cloud
HNF takes action and joins genomics revolution for CMT and rare forms of IN.
Exciting News For The CMT Patient Community
Exciting news for the CMT patient community with the first potential treatment ever!
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