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Q37295711-F9B68B13-9470-4BAA-A445-9A5B906D7928
Q37295711-F9B68B13-9470-4BAA-A445-9A5B906D7928
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http://www.wikidata.org/entity/statement/Q37295711-F9B68B13-9470-4BAA-A445-9A5B906D7928
Cell cloning-based transcriptome analysis in Rett patients: relevance to the pathogenesis of Rett syndrome of new human MeCP2 target genes.
P2860
Q37295711-F9B68B13-9470-4BAA-A445-9A5B906D7928
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http://www.wikidata.org/entity/statement/Q37295711-F9B68B13-9470-4BAA-A445-9A5B906D7928
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wasDerivedFrom
cb1aa5d58e2137582b702f2942a895115567380f
P2860
MeCP2 deficiency in Rett syndrome causes epigenetic aberrations at the PWS/AS imprinting center that affects UBE3A expression