Molecular diagnosis rate
| Inherited neuropathy clinic (n (%)) | Others (n (%)) | p Value | |
| CMT1 | 193/240 (80.4%) | 269/446 (60.3%) | <0.0001* |
| CMT2 | 29/115 (25.2%) | 44/335 (13.1%) | 0.0015* |
| ICMT | 37/62 (59.7%) | 5/23 (21.7%) | 0.001* |
| Overall CMT | 266/425 (62.6%) | 446/1182 (37.7%) | 0.003* |
↵* Fisher's exact test used; all p values significant at <0.05.
CMT, Charcot–Marie–Tooth disease; CMT1, demyelinating CMT; CMT2, axonal CMT; ICMT, intermediate CMT.