The Charcot-Marie Tooth Association (CMTA):
●Is the leading source of information about CMT for more than 25,000 patients, families and clinicians
●Offers a variety of educational materials and conferences, coordinates support and action groups in North America, and provides physician referrals and works closely with the clinical and research communities
●Is the leading financial sponsor of drug discovery research within the CMT community, and the only CMT-specific patient advocacy organization in North America, strategically aligned with the National Institutes of Health Rare Disease Clinical Research Network.
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