Ugalde Altamirano, JessicaRovira Juárez, JordiTubita, ValeriaCampistol Plana, Josep M.Poch, EstebanDiekmann, FritzPiñeiro, GastonCucchiari, DavidAzorin, SebastianBanon, ElisendaCorral Velez, VicenteTorregrosa Prats, José Vicente2025-04-022025-04-022024-05-011460-2385https://hdl.handle.net/2445/220195Comunicació/presentació a: 61st ERA Congress, The European Renal Association, Estocolm, Suècia, 23-26 maig 2024Fabry's disease (FD), a hereditary condition, is linked to the X chromosome due to a mutation in the gene encoding alpha-galactosidase A (alpha-GalA).2 p.application/pdfeng(c) Ugalde Altamirano, Jessica et al., 2024Mutació (Biologia)Malaltia de FabryInsuficiència renalMutation (Biology)Fabry's diseaseRenal insufficiencyRenal progenitor cells an early non-invasive biomarker of silent kidney injury in Fabry diseaseinfo:eu-repo/semantics/conferenceObject2024-10-15info:eu-repo/semantics/openAccess