Glomerular pathology in autosomal dominant MYH9 spectrum disorders: what are the clues telling us about disease mechanism?
Author:
Publisher
Elsevier BV
Subject
Nephrology
Reference23 articles.
1. Patients with Epstein–Fechtner syndromes owing to MYH9 R702 mutations develop progressive proteinuric renal disease;Sekine;Kidney Int,2010
2. Mutation of MYH9, encoding non-muscle myosin heavy chain A, in May-Hegglin anomaly;Kelley;Nat Genet,2000
3. Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes. The May-Hegglin/Fechtner Syndrome Consortium;Seri;Nat Genet,2000
4. MYH9 is a major-effect risk gene for focal segmental glomerulosclerosis;Kopp;Nat Genet,2008
5. CKD in MYH9-related disorders;Singh;Am J Kidney Dis,2009
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