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Q24677959-12106AC7-2E0F-49C8-9F66-53123686E2BB
Q24677959-12106AC7-2E0F-49C8-9F66-53123686E2BB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24677959-12106AC7-2E0F-49C8-9F66-53123686E2BB
DLX5 and DLX6 expression is biallelic and not modulated by MeCP2 deficiency
P2860
Q24677959-12106AC7-2E0F-49C8-9F66-53123686E2BB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24677959-12106AC7-2E0F-49C8-9F66-53123686E2BB
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Statement
wasDerivedFrom
0b084b1bdef1a60f0643357ac1cbf03a619b6562
P2860
MeCP2 deficiency in Rett syndrome causes epigenetic aberrations at the PWS/AS imprinting center that affects UBE3A expression