| http://www.w3.org/ns/prov#value | - ??? 70% have c-kit mutations (most commonly in codon 11), 15-20% have mutations in PDGFRA (most often associated with epithelioid morphology, gastric location and myxoid background), 10% are c-kit wild type and are associated with syndromes such as Neurofibromatosis - type I and Carney???s triad
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