Phenotyping of a C3-PMP22 mouse model of CMT1A 

Phenotyping of a C3-PMP22 mouse model of CMT1A 

Aug 27, 2024

Charcot-Marie Tooth (CMT) disease is a hereditary, demyelinating peripheral neuropathy, leading to progressive muscle atrophy, weakness and subsequent walking disabilities and sensory impairments. Charcot-Marie Tooth Type 1A (CMT1A) is the most common type of CMT,...