Changes

Acute Erythroid Leukemia (view source)

Revision as of 15:33, 10 May 2018

1 byte added , 15:33, 10 May 2018

Line 100: Line 100:

==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].

{| class="wikitable sortable"

Ashwiniy

285

edits