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Ebf3 protein
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Neuroblastoma SK-N-SH cells overexpressing EBF3 P177L mutation
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Literature
Most Relevant Literature
Duplication/triplication mosaicism of EBF3 and expansion of the EBF3 neurodevelopmental disorder phe…
An Integrated Phenotypic and Genotypic Approach Reveals a High-Risk Subtype Association for EBF3 Mis…
EBF3 reactivation by inhibiting the EGR1/EZH2/HDAC9 complex promotes metastasis via transcriptionall…
Clinical spectrum of individuals with de novo EBF3 variants or deletions.
Coding and noncoding variants in EBF3 are involved in HADDS and simplex autism.
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