MECP2 R133C,MECP2 D121G,MECP2 R133H,MECP2 S134F [nucleoplasm]

Stable Identifier
R-HSA-9022522
Type
Set [DefinedSet]
Species
Homo sapiens
Compartment
nucleoplasm
Locations in the PathwayBrowser
Expand all
Participants
members
Participates
as an input of
Disease
Name Identifier Synonyms
Rett syndrome DOID:1206 Rett's disorder, cerebroatrophic hyperammonemia
Cite Us!