Associated Papers
The p.R66W Variant in RAC3 Causes Severe Fetopathy Through Variant-Specific Mechanisms.
Sugawara R et al.
Cells, 2024
A missense variant at the RAC1-PAK1 binding site of RAC1 inactivates downstream signaling in VACTERL association.
Seyama R et al.
Scientific Reports, 2023
Select a paper to view details