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Additionally, mutation analysis of PRKAR1A was performed using a customized enrichment/hybrid-capture-based panel of genes recurrently altered in brain tumors ( This case represents an interesting molecular profile of an MMNST without PRKAR1A mutation, without any of the reported copy number changes, and without other previously known driver mutations
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Li Z, Jiang YY, Long C, Peng X, Tao J, Pu Y, et al
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