Gene: CFL2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1073
Gene Symbol: CFL2
CFL2 		0.110 GeneticVariation disease BEFREE To our knowledge, this is the second family in which a mutation in CFL2 causes an autosomal recessive form of congenital myopathy with features of both nemaline and myofibrillar myopathy. 22560515 2012
Entrez Id: 1073
Gene Symbol: CFL2
CFL2 		0.110 Biomarker disease HPO