Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 724066
Gene Symbol: ATXN8
ATXN8
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.010 GeneticVariation BEFREE We report the case of a 29 year old woman with a complex movement disorder syndrome due to the combination of coexisting pathological triplet repeat expansions of huntingtin and ATXN8 genes. 20403608

2010