Novel mutation inDGUOK in hepatocerebral mitochondrial DNA depletion syndrome associated with cystathioninuria
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference26 articles.
1. Mammalian deoxyribonucleoside kinases
2. Poor Storage and Handling of Tissue Mimics Mitochondrial DNA Depletion
3. Inherited Mitochondrial DNA Depletion
4. Occurrence of secondary cystathioninuria in children with inherited metabolic disorders, liver diseases, neoplasms, cystic fibrosis and celiac disease
5. Cystathioninuria and its origin in children with hepatoblastoma
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