Associated Papers
Clinicopathological features of familial fibronectin glomerulopathy caused by a splice site variant in the Fibronectin 1 gene: a case report.
Nagayama Y et al.
Cen Case Reports, 2025
Aberrant serum-derived FN1 variants bind to integrin β1 on glomerular endothelial cells contributing to thin basement membrane nephropathy.
Zhou X et al.
International Journal of Biological Macromolecules, 2024
Fibronectin glomerulopathy in an elderly patient with FN1 gene mutation: a case report and literature review.
Choi JY et al.
Bmc Nephrology, 2024
Fibronectin glomerulopathy in a kidney allograft biopsy.
Klair N et al.
Bmc Nephrology, 2023
Case Report: Recurrent Deposition in Renal Allografts: A Rare Case of Fibronectin Glomerulopathy Overlooked in Native Kidneys.
Wei X et al.
Frontiers in Genetics, 2022
Clinicopathologic Features and Outcomes in Fibronectin Glomerulopathy: A Case Series of 19 Patients.
Zhang T et al.
Frontiers in Medicine, 2020
A novel variant in FN1 in a family with fibronectin glomerulopathy.
Aslam N et al.
Human Genome Variation, 2019
Mutations in Fibronectin Cause a Subtype of Spondylometaphyseal Dysplasia with "Corner Fractures".
Lee CS et al.
American Journal of Human Genetics, 2017
Fibronectin Glomerulopathy: A Rare Autosomal Dominant Glomerular Disease.
Wu J et al.
Chinese Medical Journal, 2017
Fibronectin glomerulopathy complicated with persistent cloaca and congenital esophageal atresia: a case report and literature review.
Takii M et al.
Bmc Nephrology, 2017
Identification of mutations in FN1 leading to glomerulopathy with fibronectin deposits.
Ohtsubo H et al.
Pediatric Nephrology (berlin, Germany), 2016
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