SGCE, sarcoglycan epsilon, 8910

N. diseases: 68; N. variants: 27
Disease: Gilles de la Tourette syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0040517
Disease: Gilles de la Tourette syndrome
Gilles de la Tourette syndrome 		0.020 GeneticVariation disease BEFREE Autosomal dominant myoclonus-dystonia and Tourette syndrome in a family without linkage to the SGCE gene. 17702041 2007
CUI: C0040517
Disease: Gilles de la Tourette syndrome
Gilles de la Tourette syndrome 		0.020 GeneticVariation disease LHGDN Autosomal dominant myoclonus-dystonia and Tourette syndrome in a family without linkage to the SGCE gene. 17702041 2007
CUI: C0040517
Disease: Gilles de la Tourette syndrome
Gilles de la Tourette syndrome 		0.020 GeneticVariation disease BEFREE An association study using a polymorphism within an intron of the SGCE gene was assessed in patients with TS and OCD versus controls, and the SGCE gene itself was screened for mutations in all TS/OCD patients, followed by direct sequencing of the gene in a limited number of these patients. 15368614 2004