A novel fibrillin-1 mutation in an egyptian marfan family: A proband showing nephrotic syndrome due to focal segmental glomerulosclerosis.
Al-Haggar M, Bakr A, Wahba Y, Coucke PJ, El-Hussini F, Hafez M, Eid R, Eid AR, Sarhan A, Shaltout A, Hammad A, Yahia S, El-Rifaie A, Abdel-Hadi D.
Al-Haggar M, et al. Among authors: shaltout a.
Saudi J Kidney Dis Transpl. 2017 Jan-Feb;28(1):141-148. doi: 10.4103/1319-2442.198166.
Saudi J Kidney Dis Transpl. 2017.
PMID: 28098115
Review.