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Rao, S. V.

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    • Lee, P. L., Barton, J. C., Rao, S. V., Acton, R. T., Adler, B. K., Beutler, E. Three kinships with alas2 p520l (c. 1559 c -> t) mutation, two in association with severe iron overload, and one with sideroblastic anemia and severe iron overload Blood Cells Molecules and Diseases  2006 36:292-297  DOI:10.1016/j.bcmd.2005.12.004  PMID:16446107
    • Rao, S. V., Jollis, J. G., Harrington, R. A., Granger, C. B., Newby, L. K., Armstrong, P. W., Moliterno, D. J., Lindblad, L., Pieper, K., Topol, E. J., Stamler, J. S., Califf, R. M. Relationship of blood transfusion and clinical outcomes in patients with acute coronary syndromes JAMA-Journal of the American Medical Association  2004 292:1555-1562  DOI:10.1001/jama.292.13.1555  PMID:15467057
    • Asher, C. R., Moliterno, D. J., Bhapkar, M. V., McGuire, D. K., Rao, S. V., Holmes, D. R., Newby, L. K., Bates, E. R., Topol, E. J., Investigators, Symphony, Investigators, 2nd SYMPHONY Association of race with complications and prognosis fohowing acute coronary syndromes American Journal of Cardiology  2004 94:792-794  DOI:10.1016/j.amjcard.2004.05.069  PMID:15374792
    • Lee, P. L., Beutler, E., Rao, S. V., Barton, J. C. Genetic abnormalities and juvenile hemochromatosis: Mutations of the hjv gene encoding hemojuvelin Blood  2004 103:4669-4671  DOI:10.1182/blood-2004-01-0072  PMID:14982867

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