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Q35983002-1B6F447C-E834-4C43-8B06-2BA6B4C6D071
Q35983002-1B6F447C-E834-4C43-8B06-2BA6B4C6D071
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http://www.wikidata.org/entity/statement/Q35983002-1B6F447C-E834-4C43-8B06-2BA6B4C6D071
Mechanisms of activation of the paternally expressed genes by the Prader-Willi imprinting center in the Prader-Willi/Angelman syndromes domains.
P2860
Q35983002-1B6F447C-E834-4C43-8B06-2BA6B4C6D071
BestRank
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http://www.wikidata.org/entity/statement/Q35983002-1B6F447C-E834-4C43-8B06-2BA6B4C6D071
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wasDerivedFrom
af3c5cf3cd381a3567970d30a411ab0239c0f433
P2860
MeCP2 deficiency in Rett syndrome causes epigenetic aberrations at the PWS/AS imprinting center that affects UBE3A expression