Gene: ATXN8 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 724066
Gene Symbol: ATXN8
ATXN8 		0.010 GeneticVariation group 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