KPNA7, karyopherin subunit alpha 7, 402569

N. diseases: 13; N. variants: 8
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3887898
Disease: Infantile Spasm
Infantile Spasm
0.010 GeneticVariation disease BEFREE Autosomal recessive mutations in nuclear transport factor KPNA7 are associated with infantile spasms and cerebellar malformation. 24045845 2014