An international MDA-supported study will identify genetic modifiers of CMT1A and determine additional genetic causes of CMT in general

posted on October 24, 2011 - 2:30pm
Researchers supported in part by MDA are seeking people with Charcot-Marie-Tooth disease (CMT) to participate in a study to identify genetic modifiers of the type 1A form of CMT (CMT1A) and determine previously unknown genetic causes of CMT.

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