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Q36959606-17C5D683-CC72-4407-82A9-37959E45BE84
Q36959606-17C5D683-CC72-4407-82A9-37959E45BE84
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36959606-17C5D683-CC72-4407-82A9-37959E45BE84
MECP2 genomic structure and function: insights from ENCODE
P2860
Q36959606-17C5D683-CC72-4407-82A9-37959E45BE84
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36959606-17C5D683-CC72-4407-82A9-37959E45BE84
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wasDerivedFrom
4e8a24ed07807ec7b88fdb6075e6e5755c8ce471
P2860
MeCP2 deficiency in Rett syndrome causes epigenetic aberrations at the PWS/AS imprinting center that affects UBE3A expression