MECP2 mutants P302R,K304E,K305R,R306C,(R306H) [nucleoplasm]

Stable Identifier
R-HSA-9005540
Type
Set [CandidateSet]
Species
Homo sapiens
Compartment
Locations in the PathwayBrowser
Participants
Participant Of
Disease
Name Identifier Synonyms
Rett syndrome 1206 Rett's disorder, cerebroatrophic hyperammonemia