Disease: Familial Periodic Paralysis ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0030443
Disease: Familial Periodic Paralysis
Familial Periodic Paralysis 		0.010 Biomarker disease BEFREE Novel mutations in human and mouse SCN4A implicate AMPK in myotonia and periodic paralysis. 25348630 2014