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Investigaciones

Complete thyroxine binding globulin deficiency due to a novel p.A64D mutation, associated with increased affinity in Transthyretin (p.A109T mutation) in an hypothyroid patient

Sklate R., Maccallini GC., Olcese M., Agûero M., Sánchez M., González Sarmineto R., Targovnik H., Niepomniszcze H., Rivolta C.
14th International Thyroid Congress, París (Francia), septiembre 2010.