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KCNQ1 binds spn-A. 2 / 2

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"The CAGA haplotype more frequent among BWS patients was associated with loss of methylation of an exon 10 DMR (KvDMR1) in the maternally imprinted KCNQ1 gene ( xref )."

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sparser

"Premature termination of Kcnq1ot1 was found to alter chromatin conformation capture (3C) interactions in the mouse heart ( xref , xref , xref ) and, more directly, Kcnq1ot1 silencing abrogates a long-range interaction between the DMR and the Kcnq1 promoter ( xref )."

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IndraLab

Statements

KCNQ1 binds spn-A. 2 / 2

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