Gene: OPA3 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 80207
Gene Symbol: OPA3
OPA3 		0.010 GeneticVariation phenotype BEFREE We identify a novel missense mutation in OPA3 as the cause of a complex neurological disorder, expanding the OPA3 -linked phenotype by early-onset pyramidal tract signs and marked lower limb dystonia. 23700088 2013