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Description
Its deficiency is associated with the risk of GI epithelial defect and IBD
24 These mutations serve as key molecular discriminators between glioma subtypes and are highly prevalent in lower-grade diffuse gliomas (WHO grades IIIII) and secondary GBMs 25 but are largely absent in primary GBMs, which are predominantly IDH wild-type
doi: 10.1093/ndt/gfh807
Article PubMed PubMed Central Google Scholar Wakeman, S
