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Q37000934-35FC427C-9655-49AB-8C1A-6E6C2FA20D1A
Q37000934-35FC427C-9655-49AB-8C1A-6E6C2FA20D1A
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Statement
http://www.wikidata.org/entity/statement/Q37000934-35FC427C-9655-49AB-8C1A-6E6C2FA20D1A
Smchd1 regulates a subset of autosomal genes subject to monoallelic expression in addition to being critical for X inactivation
P2860
Q37000934-35FC427C-9655-49AB-8C1A-6E6C2FA20D1A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37000934-35FC427C-9655-49AB-8C1A-6E6C2FA20D1A
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wasDerivedFrom
55912401093c66513801cb0f910fb2a426dbaa11
P2860
MeCP2 deficiency in Rett syndrome causes epigenetic aberrations at the PWS/AS imprinting center that affects UBE3A expression