Gene: FBXL4 ×
Source: CLINVAR ×
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 26235
Gene Symbol: FBXL4
FBXL4 		0.100 GeneticVariation phenotype CLINVAR FBXL4 defects are common in patients with congenital lactic acidemia and encephalomyopathic mitochondrial DNA depletion syndrome. 27743463 2017
Entrez Id: 26235
Gene Symbol: FBXL4
FBXL4 		0.100 GeneticVariation phenotype CLINVAR Clinical, morphological, biochemical, imaging and outcome parameters in 21 individuals with mitochondrial maintenance defect related to FBXL4 mutations. 25868664 2015