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RT @edgarvlermamd: @kdjhaveri @hswapnil @Kidney_Int Familial SSINS due to Minimal Change Disease is extremely rare and no genetic defect ha…
RT @edgarvlermamd: @kdjhaveri @hswapnil @Kidney_Int Familial SSINS due to Minimal Change Disease is extremely rare and no genetic defect ha…
@kdjhaveri @hswapnil @Kidney_Int Familial SSINS due to Minimal Change Disease is extremely rare and no genetic defect has been identified so far ca. 2013 from @BioMedCentral #Nephpearls #AskRenal 👉🏼 https://t.co/NspCfbiOW2 https://t.co/Ys3M6wGfFZ