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Q22337143-93F43033-ADD3-4A02-9243-687D793954FE
Q22337143-93F43033-ADD3-4A02-9243-687D793954FE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q22337143-93F43033-ADD3-4A02-9243-687D793954FE
Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3.
P2860
Q22337143-93F43033-ADD3-4A02-9243-687D793954FE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q22337143-93F43033-ADD3-4A02-9243-687D793954FE
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Statement
wasDerivedFrom
52c52cef94481572111f69e93bfed6085f6f0b27
P2860
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2