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P0097IDENTIFICATION OF TWO NOVELS SINGLE NUCLEOTIDE VARIANTS OF THE COMPLEMENT GENES IN A PATIENT WITH THE ASSOCIATION OF PREGNANCY ATYPICAL HEMOLYTIC UREMIC SYNDROME AND C3 GLOMERULOPATHY
GRELONI, GUSTAVO, Varela, Federico, Bratti, Griselda, Rosa Diez, Guillermo, Dos Santos, Celia, Sanchez Luceros, AnaliaVolume:
35
Journal:
Nephrology Dialysis Transplantation
DOI:
10.1093/ndt/gfaa142.P0097
Date:
June, 2020
File:
PDF, 105 KB
2020