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Q35629499-4103625B-0300-418F-B0BF-7C3D2AAE45A9
Q35629499-4103625B-0300-418F-B0BF-7C3D2AAE45A9
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http://www.wikidata.org/entity/statement/Q35629499-4103625B-0300-418F-B0BF-7C3D2AAE45A9
Partial rescue of MeCP2 deficiency by postnatal activation of MeCP2.
P2860
Q35629499-4103625B-0300-418F-B0BF-7C3D2AAE45A9
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35629499-4103625B-0300-418F-B0BF-7C3D2AAE45A9
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wasDerivedFrom
00413e7c3a6874be974e0bf30a3bd60b3169c053
P2860
MeCP2 deficiency in Rett syndrome causes epigenetic aberrations at the PWS/AS imprinting center that affects UBE3A expression