PKN1, protein kinase N1, 5585

N. diseases: 48; N. variants: 3
Disease: Muscular Dystrophy ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0026850
Disease: Muscular Dystrophy
Muscular Dystrophy 		0.010 GeneticVariation disease BEFREE As the mouse mutation myodystrophy myd has been mapped to the same region, Prkcl1 is a candidate gene for myd. 9570957 1998