Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4168
Gene Symbol: MCF2
MCF2
CUI: C1845668
Disease: Perisylvian syndrome
Perisylvian syndrome
0.010 GeneticVariation BEFREE Strikingly, we find that the CBPS-associated MCF2 mutation impairs cortical laminar positioning, supporting the hypothesis that alterations in the process of embryonic neuronal migration can lead to rare cases of CBPS. 31846234

2020