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About this Biochemistry, Genetics and Molecular Biology article
Mutations in human DNA polymerase confer unique mechanisms of catalytic deficiency that mirror the disease severity in mitochondrial disorder patients by Sohl, C. D.; Kasiviswanathan, R.; Copeland, W. C.; Anderson, K. S. is a Biochemistry, Genetics and Molecular Biology article available to read on EtoBox.
It is typically read by researchers, students, and practitioners in Biochemistry, Genetics and Molecular Biology.
- Author
- Sohl, C. D.; Kasiviswanathan, R.; Copeland, W. C.; Anderson, K. S.
- Publisher
- Oxford University Press; Oxford University Press (OUP) (ISSN 0964-6906)
- Published
- 2012
- Language
- EN
- Field
- Biochemistry, Genetics and Molecular Biology (Life Sciences)
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