Aggarwal, M., & Brosh, R. M. (2009). WRN helicase defective in the premature aging disorder Werner syndrome genetically interacts with topoisomerase 3 and restores the top3 slow growth phenotype of sgs1 top3. Impact Journals LLC.
Style de citation ChicagoAggarwal, Monika, et Robert M. Brosh. WRN Helicase Defective in the Premature Aging Disorder Werner Syndrome Genetically Interacts With Topoisomerase 3 and Restores The Top3 Slow Growth Phenotype of Sgs1 Top3. Impact Journals LLC, 2009.
Style de citation MLAAggarwal, Monika, et Robert M. Brosh. WRN Helicase Defective in the Premature Aging Disorder Werner Syndrome Genetically Interacts With Topoisomerase 3 and Restores The Top3 Slow Growth Phenotype of Sgs1 Top3. Impact Journals LLC, 2009.