awgldk
/
wikidata
/
Login
Register
TriplyDB
Wikidata
Browser
Table
SPARQL
Graphs
1
1
Services
1
1
Assets
0
0
Insights
Schema
BETA
Class frequency
Class hierarchy
10.22.2581
10.22.2581
http://dx.doi.org/10.1093/HMG/10.22.2581
Familial and sporadic forms of central core disease are associated with mutations in the C-terminal domain of the skeletal muscle ryanodine receptor.
P356
Q43800108-80FAE4EF-25AD-43D6-AC23-F4E5ADD2473F
P356
10.22.2581
http://dx.doi.org/10.1093/HMG/10.22.2581