Deoxypyrimidine monophosphate bypass therapy for thymidine kinase 2 deficiency

Autosomal recessive mutations in the thymidine kinase 2 gene (TK2) cause mitochondrial DNA depletion, multiple deletions, or both due to loss of TK2 enzyme activity and ensuing unbalanced deoxynucleotide triphosphate (dNTP) pools. To bypass Tk2 deficiency, we administered deoxycytidine and deoxythym...

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Detalles Bibliográficos
Autores principales: Garone, Caterina, Garcia-Diaz, Beatriz, Emmanuele, Valentina, Lopez, Luis C, Tadesse, Saba, Akman, Hasan O, Tanji, Kurenai, Quinzii, Catarina M, Hirano, Michio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BlackWell Publishing Ltd 2014
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4154130/
https://www.ncbi.nlm.nih.gov/pubmed/24968719
http://dx.doi.org/10.15252/emmm.201404092

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4154130/
https://www.ncbi.nlm.nih.gov/pubmed/24968719
http://dx.doi.org/10.15252/emmm.201404092

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