PubMed:19394258 / 0-238 21 Projects
Annnotations
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 0-101 | Sentence | denotes | The first founder DGUOK mutation associated with hepatocerebral mitochondrial DNA depletion syndrome. |
| T2 | 102-235 | Sentence | denotes | Deoxyguanosine kinase (dGK) deficiency is a frequent cause of mitochondrial DNA depletion associated with a hepatocerebral phenotype. |