Publication | Open Access
Paternal gender specificity and mild phenotypes in Charcot–Marie–Tooth type 1A patients with de novo 17p12 rearrangements
11
Citations
27
References
2020
Year
This study suggests that de novo CMT1A patients tend to have milder symptoms and that the paternal ages at child births in the de novo group are higher than those of the non-de novo group.
| Year | Citations | |
|---|---|---|
Page 1
Page 1