Pathologic-genomic correlation identified a novel variant in FN1 and established the diagnosis of recurrent fibronectin glomerulopathy in the kidney allograft.

Batal, Ibrahim; Nasr, Samih H; Dasari, Surendra; Weins, Astrid; Vena, Natalie; Stokes, Michael B; Kiryluk, Krzysztof; Appel, Gerald B

Batal, Ibrahim; Nasr, Samih H; Dasari, Surendra; Weins, Astrid; Vena, Natalie; Stokes, Michael B; Kiryluk, Krzysztof; Appel, Gerald B.

Affiliation

Batal I; Department of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, New York, USA. Electronic address: ib234@cumc.columbia.edu.
Nasr SH; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA.
Dasari S; Department of Health Science Research, Mayo Clinic, Rochester, Minnesota, USA.
Weins A; Department of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts, USA.
Vena N; Division of Nephrology, Department of Medicine, Columbia University Irving Medical Center, New York, New York, USA.
Stokes MB; Department of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, New York, USA.
Kiryluk K; Division of Nephrology, Department of Medicine, Columbia University Irving Medical Center, New York, New York, USA.
Appel GB; Division of Nephrology, Department of Medicine, Columbia University Irving Medical Center, New York, New York, USA.

Am J Transplant ; 24(3): 498-502, 2024 Mar.

Article in En | MEDLINE | ID: mdl-37852577

Subject(s)
Key words

fibronectin glomerulopathy; genetics; pathology

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Glomerulonephritis, Membranoproliferative / Glomerulonephritis, IGA Limits: Humans Language: En Journal: Am J Transplant Journal subject: TRANSPLANTE Year: 2024 Document type: Article Country of publication:

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