Gene: XRCC1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7515
Gene Symbol: XRCC1
XRCC1 		0.010 GeneticVariation disease BEFREE Here we show that biallelic mutations in the human XRCC1 gene are associated with ocular motor apraxia, axonal neuropathy, and progressive cerebellar ataxia. 28002403 2017