Gene: SLC19A3 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 80704
Gene Symbol: SLC19A3
SLC19A3 		0.010 GeneticVariation disease BEFREE Homozygous or compound heterozygous mutations in SLC19A3 cause two distinct clinical phenotypes, biotin-responsive basal ganglia disease and Wernicke's-like encephalopathy. 21176162 2010