Answers are grounded in this paper and cite their sources.
Deoxyguanosine kinase (DGUOK) gene mutations have been identified in the hepatocerebral form of mitochondrial DNA depletion syndromes. We report here clinical and laboratory features of 3 infants with novel DGUOK gene mutations, c.130G>A (Glu44Lys), c.493G>A (Glu165Lys), and c.707+3_6delTAAG.
No takes yet. Share an insight, caveat, or question.
Sezer et al. (2014) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: