v1
Myelin uncompaction in Charcot-Marie-Tooth neuropathy type 1A with a point mutation of peripheral myelin protein-22.
Identifier:nobleid.org/w1/20260515/AD2CC651
Type:Journal Article
0 views
Embeddable Badge
[](https://nobleid.org/work/w1/20260515/AD2CC651)
Bibliometric Analysis
Impact metrics, research fronts, co-authorship networks →
Authors & Claims