Clinical and molecular characterization of a family with a dominant renin gene mutation and response to treatment with fludrocortisone

Por Bleyer, A.J., Živná, M., Hulková, H., Hodanová, K., Vyletal, P., Sikora, J., Živný, J., Sovová, J., Hart, T.C., Adams, J.N., Elleder, M., Kapp, K., Haws, R., Cornell, L.D., Kmoch, S., Hart, P.S.
Publicado no Clin Nephrol (2010)