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Acute Erythroid Leukemia (view source)

Revision as of 15:21, 10 May 2018

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→‎Gene Mutations (SNV/INDEL)

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==Gene Mutations (SNV/INDEL)==

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~~Not Applicable~~

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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].

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Ashwiniy

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