A novel fibrillin-1 mutation in an egyptian marfan family: A proband showing nephrotic syndrome due to focal segmental glomerulosclerosis-Reference-Cited by-同舟云学术

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A novel fibrillin-1 mutation in an egyptian marfan family: A proband showing nephrotic syndrome due to focal segmental glomerulosclerosis

Published:2017 Issue:1 Volume:28 Page:141
ISSN:1319-2442
Container-title:Saudi Journal of Kidney Diseases and Transplantation
language:en
Short-container-title:Saudi J Kidney Dis Transpl

Author:

Al-Haggar Mohammad,Bakr Ashraf,Wahba Yahya,Coucke PaulJ,El-Hussini Fatma,Hafez Mona,Eid Riham,Eid Abdel-Rahman,Sarhan Amr,Shaltout Ali,Hammad Ayman,Yahia Sohier,El-Rifaie Ahmad,Abdel-Hadi Dina

Publisher

Medknow

Subject

General Medicine

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Extracellular matrix and vascular dynamics in the kidney of a murine model for Marfan syndrome;PLOS ONE;2023-05-09

2. Features of Marfan syndrome not listed in the Ghent nosology – the dark side of the disease;Expert Review of Cardiovascular Therapy;2019-12-02

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