Gene: FBXL4 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 26235
Gene Symbol: FBXL4
FBXL4 		0.110 GeneticVariation disease BEFREE FBXL4 mutations are a recurrent cause of mitochondrial encephalomyopathy onset in early infancy. 23993194 2013
Entrez Id: 26235
Gene Symbol: FBXL4
FBXL4 		0.110 GeneticVariation disease CLINVAR