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Q37277208-33DC79B6-74D7-4F12-90BE-E2334F9C0CAA
Q37277208-33DC79B6-74D7-4F12-90BE-E2334F9C0CAA
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http://www.wikidata.org/entity/statement/Q37277208-33DC79B6-74D7-4F12-90BE-E2334F9C0CAA
Mutation of a single CTCF target site within the H19 imprinting control region leads to loss of Igf2 imprinting and complex patterns of de novo methylation upon maternal inheritance.
P2860
Q37277208-33DC79B6-74D7-4F12-90BE-E2334F9C0CAA
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Statement
http://www.wikidata.org/entity/statement/Q37277208-33DC79B6-74D7-4F12-90BE-E2334F9C0CAA
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wasDerivedFrom
b1872c12aea3d36de212f08d6d06b5e21ba1ad0e
P2860
A paternal-specific methylation imprint marks the alleles of the mouse H19 gene.