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Q47605915-3F8D404A-E34B-4FB8-A1FA-99D6C9748F11
Q47605915-3F8D404A-E34B-4FB8-A1FA-99D6C9748F11
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Statement
http://www.wikidata.org/entity/statement/Q47605915-3F8D404A-E34B-4FB8-A1FA-99D6C9748F11
MeCP2_E1 N-terminal modifications affect its degradation rate and are disrupted by the Ala2Val Rett mutation.
P2860
Q47605915-3F8D404A-E34B-4FB8-A1FA-99D6C9748F11
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47605915-3F8D404A-E34B-4FB8-A1FA-99D6C9748F11
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wasDerivedFrom
48b3e64f89ad6ba167dd335a0c5c45405e12a61e
P2860
Methyl CpG-binding protein isoform MeCP2_e2 is dispensable for Rett syndrome phenotypes but essential for embryo viability and placenta development.