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LAMA2 and LOXL4 are candidate FSGS genes.
Vijayan P, Hack S, Yao T, Qureshi MA, Paterson AD, John R, Davenport B, Lennon R, Pei Y, Barua M. Vijayan P, et al. BMC Nephrol. 2021 Sep 26;22(1):320. doi: 10.1186/s12882-021-02524-6. BMC Nephrol. 2021. PMID: 34565340 Free PMC article.
A Rare Autosomal Dominant Variant in Regulator of Calcineurin Type 1 (RCAN1) Gene Confers Enhanced Calcineurin Activity and May Cause FSGS.
Lane BM, Murray S, Benson K, Bierzynska A, Chryst-Stangl M, Wang L, Wu G, Cavalleri G, Doyle B, Fennelly N, Dorman A, Conlon S, Vega-Warner V, Fermin D, Vijayan P, Qureshi MA, Shril S, Barua M, Hildebrandt F, Pollak M, Howell D, Sampson MG, Saleem M, Conlon PJ, Spurney R, Gbadegesin R. Lane BM, et al. Among authors: vijayan p. J Am Soc Nephrol. 2021 Jul;32(7):1682-1695. doi: 10.1681/ASN.2020081234. Epub 2021 Apr 16. J Am Soc Nephrol. 2021. PMID: 33863784 Free PMC article.
79 results