Title : Mutant mitochondrial thymidine kinase in mitochondrial DNA depletion myopathy.

Pub. Date : 2001 Nov

PMID : 11687801






1 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 Mutations in TK2 represent a new etiology for mitochondrial DNA depletion, underscoring the importance of the mitochondrial dNTP pool in the pathogenesis of mitochondrial depletion. Parathion thymidine kinase 2 Homo sapiens