Genotype and Outcome After Kidney Transplantation in Alport Syndrome
Author:
Publisher
Elsevier BV
Subject
Nephrology
Reference34 articles.
1. Making the diagnosis of Alport’s syndrome;Pirson;Kidney Int,1999
2. The clinical spectrum of type IV collagen mutations;Lemmink;Hum Mutat,1997
3. Identification of mutations in the alpha 3(IV) and alpha 4(IV) collagen genes in autosomal recessive Alport syndrome;Mochizuki;Nat Genet,1994
4. Mutations in the type IV collagen alpha 3 (COL4A3) gene in autosomal recessive Alport syndrome;Lemmink;Hum Mol Genet,1994
5. Autosomal dominant Alport syndrome caused by a COL4A3 splice site mutation;van der Loop;Kidney Int,2000
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1. De novo glomerulonephritis associated with IgA anti-GBM alloantibodies after kidney transplantation in Alport syndrome: A case report with diagnostic implications;Clinical Immunology;2024-11
2. Four novel mutations identified in the COL4A3, COL4A4 and COL4A5 genes in 10 families with Alport syndrome;BMC Medical Genomics;2024-07-08
3. Developing a genetic testing panel for evaluation of morbidities in kidney transplant recipients;Kidney International;2024-07
4. Explaining Alport syndrome—lessons from the adult nephrology clinic;Journal of Rare Diseases;2024-05-13
5. Monogenic Kidney Diseases in Kidney Transplantation;Kidney International Reports;2023-12
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