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Coinheritance of COL4A5 and MYO1E mutations accentuate the severity of kidney disease.
Lennon R, Stuart HM, Bierzynska A, Randles MJ, Kerr B, Hillman KA, Batra G, Campbell J, Storey H, Flinter FA, Koziell A, Welsh GI, Saleem MA, Webb NJ, Woolf AS. Lennon R, et al. Pediatr Nephrol. 2015 Sep;30(9):1459-65. doi: 10.1007/s00467-015-3067-9. Epub 2015 Mar 5. Pediatr Nephrol. 2015. PMID: 25739341 Free PMC article.
The importance of clinician, patient and researcher collaborations in Alport syndrome.
Rheault MN, Savige J, Randles MJ, Weinstock A, Stepney M, Turner AN, Parziale G, Gross O, Flinter FA, Miner JH, Lagas S, Gear S, Lennon R. Rheault MN, et al. Among authors: lennon r. Pediatr Nephrol. 2020 May;35(5):733-742. doi: 10.1007/s00467-019-04241-7. Epub 2019 May 1. Pediatr Nephrol. 2020. PMID: 31044288 Free PMC article.
584 results