Taxonomy

CMT2D Research

CMT2D The CMT 2D locus is on chromosome 7p14 and

CMT4 Research

CMT4 Below we share with you the research projects the

CMT1X Research

CMT1X CMT1X is the second most common form of CMT,

CMT1B Research

CMT1B This CMT subtype is caused by mutations in the

SORD Research

SORD Research Every year more types of CMT are identified

CMT2E Research

CMT2E CMT2E is caused by dominant mutations in the neurofilament

CMT2A Research

CMT2A CMT2A is caused by dominant mutations in Mitofusin 2

CMTA-STAR Research for Demyelinating Forms of CMT

DEMYELINATING FORMS OF CMT (Types 1, 4 and X) The

CMTA-STAR Research for Axonal Forms of CMT

AXONAL FORMS OF CMT (Type 2 and Unidentified/SORD) The CMTA’s

CMTA Preclinical Testing Network

fast and cost-effective pre-clinical evaluation of therapeutics The Bio International