IndraLab

Statements


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"These functional associations of IGF2 and KCNQ1 rely on publications reporting how a differentially methylated region in KCNQ1 controls imprinted expression of other genes in the neighborhood xref and about epigenetic abnormalities in the IGF2/H19 region of Beckwith-Wiedemann syndrome patients xref ."

sparser
"Our results suggest that the aberrant methylation of IGF2 and KCNQ1 genes may be associated with sperm DNA damage."