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Q40492792-D54839BE-A928-4C8E-8CBC-88F92A8DF967
Q40492792-D54839BE-A928-4C8E-8CBC-88F92A8DF967
BestRank
Statement
http://www.wikidata.org/entity/statement/Q40492792-D54839BE-A928-4C8E-8CBC-88F92A8DF967
Beckwith-Wiedemann syndrome caused by maternally inherited mutation of an OCT-binding motif in the IGF2/H19-imprinting control region, ICR1.
P2860
Q40492792-D54839BE-A928-4C8E-8CBC-88F92A8DF967
BestRank
Statement
http://www.wikidata.org/entity/statement/Q40492792-D54839BE-A928-4C8E-8CBC-88F92A8DF967
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
d2c24698fc8ba54f3cb0de2e456c87ab08e83730
P2860
A dyad oct-binding sequence functions as a maintenance sequence for the unmethylated state within the H19/Igf2-imprinted control region.