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Q24594577-20A4BEF1-FA29-4697-BDCC-F0C3D4CD9F4E
Q24594577-20A4BEF1-FA29-4697-BDCC-F0C3D4CD9F4E
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http://www.wikidata.org/entity/statement/Q24594577-20A4BEF1-FA29-4697-BDCC-F0C3D4CD9F4E
The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13
P2860
Q24594577-20A4BEF1-FA29-4697-BDCC-F0C3D4CD9F4E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24594577-20A4BEF1-FA29-4697-BDCC-F0C3D4CD9F4E
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wasDerivedFrom
6c701d9dcc74f9e93c1f119caf1c328e3d88def9
P2860
MeCP2 deficiency in Rett syndrome causes epigenetic aberrations at the PWS/AS imprinting center that affects UBE3A expression