Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleA Novel Fibrillin–1 Mutation in an Egyptian Marfan Family: A Proband Showing Nephrotic Syndrome Due to Focal Segmental Glomerulosclerosis.AuthorsAl-Haggar, Mohammad; Bakr, Ashraf; Wahba, Yahya; Coucke, Paul J.; El-Hussini, Fatma; Hafez, Mona; Eid, Riham; Eid, Abdel-Rahman; Sarhan, Amr; Shaltout, Ali; Hammad, Ayman; Yahia, Sohier; El-Rifaie, Ahmad; Abdel-Hadi, DinaPublicationSaudi Journal of Kidney Diseases & Transplantation, 2017, Vol 28, Issue 1, p141ISSN1319-2442Publication typeArticleDOI10.4103/1319-2442.198166