Gene: SPG11 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 80208
Gene Symbol: SPG11
SPG11 		0.030 GeneticVariation disease BEFREE Identification of new mutations in the SPG11 gene, validating its implication in Kjellin's syndrome. 21035867 2011
Entrez Id: 80208
Gene Symbol: SPG11
SPG11 		0.030 GeneticVariation disease BEFREE SPG11 mutations cause Kjellin syndrome, a hereditary spastic paraplegia with thin corpus callosum and central retinal degeneration. 19194956 2009
Entrez Id: 80208
Gene Symbol: SPG11
SPG11 		0.030 Biomarker disease BEFREE The neurological and radiological findings in SPG11 and SPG15 patients were relatively similar. 18332254 2008