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Q30575472-6C202B7B-F0F0-471B-AD33-38862B853297
Q30575472-6C202B7B-F0F0-471B-AD33-38862B853297
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30575472-6C202B7B-F0F0-471B-AD33-38862B853297
Mice with an isoform-ablating Mecp2 exon 1 mutation recapitulate the neurologic deficits of Rett syndrome.
P2860
Q30575472-6C202B7B-F0F0-471B-AD33-38862B853297
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30575472-6C202B7B-F0F0-471B-AD33-38862B853297
rank
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wasDerivedFrom
432dde669d39ffe9b9dd2e18eb40dabd027e7a29
P2860
Methyl CpG-binding protein isoform MeCP2_e2 is dispensable for Rett syndrome phenotypes but essential for embryo viability and placenta development.