Associated Papers
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
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