Associated Papers
Molecular Dynamics Simulations of the SPRED2Leu100Pro EVH-1 Domain Complexed with the GAP-Related Domain of Neurofibromin.
Terrusa M et al.
International Journal of Molecular Sciences, 2025
A Novel Homozygous Loss-of-Function Variant in SPRED2 Causes Autosomal Recessive Noonan-like Syndrome.
Onore ME et al.
Genes, 2023
SPRED2 loss-of-function causes a recessive Noonan syndrome-like phenotype.
Motta M et al.
American Journal of Human Genetics, 2021
Select a paper to view details