KIF2A, kinesin family member 2A, 3796

N. diseases: 81; N. variants: 29
Disease: Classical Lissencephaly ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0431375
Disease: Classical Lissencephaly
Classical Lissencephaly 		0.010 GeneticVariation disease BEFREE This report also establishes that KIF2A mutations represent significant causes of classic lissencephaly with microcephaly. 27747449 2017