Identification of a novel UMOD mutation (c.163G>A) in a Brazilian family with autosomal dominant tubulointerstitial kidney disease

Por Lopes, L.B., Abreu, C.C., Souza, C.F., Guimaraes, L.E.R., Silva, A.A., Aguiar-Alves, F., Kidd, K.O., Kmoch, S., Bleyer, A.J., Almeida, J.R.
Publicado no Braz J Med Biol Res (2018)

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)