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Q35684394-A0D6189B-4BC8-43A0-A9FC-2D9D6D09BFEB
Q35684394-A0D6189B-4BC8-43A0-A9FC-2D9D6D09BFEB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35684394-A0D6189B-4BC8-43A0-A9FC-2D9D6D09BFEB
MECP2, a gene associated with Rett syndrome in humans, shows conserved coding regions, independent Alu insertions, and a novel transcript across primate evolution
P2860
Q35684394-A0D6189B-4BC8-43A0-A9FC-2D9D6D09BFEB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35684394-A0D6189B-4BC8-43A0-A9FC-2D9D6D09BFEB
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Statement
wasDerivedFrom
e10480d85d434121bd77221f16424ee87c0eace0
P2860
Methyl CpG-binding protein isoform MeCP2_e2 is dispensable for Rett syndrome phenotypes but essential for embryo viability and placenta development.