What does it mean when a nerve conduction pattern falls between demyelinating and axonal CMT? Meet CMTRIE, a new type of CMT caused by mutations in the KCTD11 gene.
CMTA Presents New Genetic Landscape Analysis at The 2025 Annual Meeting of the Peripheral Nerve Society
The Charcot-Marie-Tooth Association (CMTA), the largest philanthropic funder of Charcot-Marie-Tooth (CMT) disease research, presented a...
Long Read Sequencing in Undiagnosed Axonal CMT Patients
The answer is hiding in your DNA. For some, it hasn’t been found yet. This CMTA-funded study uses long-read sequencing to uncover genetic causes of CMT that standard tests may miss.
Solve-CMT Resource: Addressing the Diagnostic Gap and Drug Target Discovery via Advanced Genomics
What happens when CMTA-supported scientists use AI to analyze thousands of CMT genomes for undiscovered genes?
