Pub. Date : 2016
PMID : 26863430
2 Functional Relationships(s)Download |
Sentence | Compound Name | Protein Name | Organism |
| 1 | Novel SLC19A3 Promoter Deletion and Allelic Silencing in Biotin-Thiamine-Responsive Basal Ganglia Encephalopathy. | Thiamine | solute carrier family 19 member 3 | Homo sapiens |
| 2 | BACKGROUND: Biotin-thiamine responsive basal ganglia disease is a severe, but potentially treatable disorder caused by mutations in the SLC19A3 gene. | Thiamine | solute carrier family 19 member 3 | Homo sapiens |