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References Sikiric P, Seiwerth S, Rucman R, et al
WASF3 belongs to a family of genes with homology to the WiskottAldrich Syndrome (WAS) gene which when mutated can cause the rare X-linked immunodeficiency disorder associated with B cell dysfunction (65)
Blood-brain-barrier spheroids as an in vitro screening platform for brain-penetrating agents
