v1
Variable brain phenotype primarily affects the brainstem and cerebellum in patients with osteogenesis imperfecta caused by recessive WNT1 mutations.
Identifier:nobleid.org/w1/20260526/1758AFDA
Type:Journal Article
0 views
Embeddable Badge
[](https://nobleid.org/work/w1/20260526/1758AFDA)
Bibliometric Analysis
Impact metrics, research fronts, co-authorship networks →
Authors & Claims