FGF13, fibroblast growth factor 13, 2258

N. diseases: 167; N. variants: 1
Disease: Malformations of Cortical Development, Group II ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1837249
Disease: Malformations of Cortical Development, Group II
Malformations of Cortical Development, Group II 		0.010 GeneticVariation disease BEFREE Genetic deletion of FGF13 in mice results in neuronal migration defects in both the neocortex and the hippocampus. 22726441 2012