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→Gene Mutations (SNV/INDEL)
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==Gene Mutations (SNV/INDEL)==
==Gene Mutations (SNV/INDEL)==
−Intraclonal heterogeneity and founder mutations of TP53 were reported in 92% (11 out of 12 cases) while co-occurrence of TP53 mutation and deletion due to chromosome 17p abnormalities was detected in 73% of PEL cases [13].
+Intraclonal heterogeneity and founder mutations of TP53 were reported in 92% (11 out of 12 cases) while co-occurrence of TP53 mutation and deletion due to chromosome 17p abnormalities were detected in 73% of PEL cases [13].
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