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Q35922196-39F4FFEF-D952-4A64-AE58-A35E27A95DF2
Q35922196-39F4FFEF-D952-4A64-AE58-A35E27A95DF2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35922196-39F4FFEF-D952-4A64-AE58-A35E27A95DF2
Methyl CpG-binding protein isoform MeCP2_e2 is dispensable for Rett syndrome phenotypes but essential for embryo viability and placenta development.
P2860
Q35922196-39F4FFEF-D952-4A64-AE58-A35E27A95DF2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35922196-39F4FFEF-D952-4A64-AE58-A35E27A95DF2
rank
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Statement
wasDerivedFrom
ba960380e3b15ba7fbc525465978c99b1066d4b4
P2860
A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome