Associated Papers
Syndromic craniosynostosis caused by a novel missense variant in MAP4K4: Expanding the genotype-phenotype relationship in RASopathies.
Yoon JG et al.
Clinical Genetics, 2024
Abrogation of MAP4K4 protein function causes congenital anomalies in humans and zebrafish.
Patterson V et al.
Science Advances, 2023
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