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Mutations in human DNA polymerase confer unique mechanisms of catalytic deficiency that mirror the disease severity in mitochondrial disorder patients
Sohl, C. D., Kasiviswanathan, R., Copeland, W. C., Anderson, K. S.Volume:
22
Language:
english
Journal:
Human Molecular Genetics
DOI:
10.1093/hmg/dds509
Date:
March, 2013
File:
PDF, 397 KB
english, 2013