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

Stable Identifier
R-HSA-9022522
Type
Set [DefinedSet]
Species
Homo sapiens
Compartment
Locations in the PathwayBrowser
Participants
Participant Of
Disease
Name Identifier Synonyms
Rett syndrome 1206 Rett's disorder, cerebroatrophic hyperammonemia