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The EAHAD blood coagulation factor VII variant database.
Giansily-Blaizot M, Rallapalli PM, Perkins SJ, Kemball-Cook G, Hampshire DJ, Gomez K, Ludlam CA, McVey JH. Giansily-Blaizot M, et al. Among authors: rallapalli pm. Hum Mutat. 2020 Jul;41(7):1209-1219. doi: 10.1002/humu.24025. Epub 2020 Apr 29. Hum Mutat. 2020. PMID: 32333443
Statistical Validation of Rare Complement Variants Provides Insights into the Molecular Basis of Atypical Hemolytic Uremic Syndrome and C3 Glomerulopathy.
Osborne AJ, Breno M, Borsa NG, Bu F, Frémeaux-Bacchi V, Gale DP, van den Heuvel LP, Kavanagh D, Noris M, Pinto S, Rallapalli PM, Remuzzi G, Rodríguez de Cordoba S, Ruiz A, Smith RJH, Vieira-Martins P, Volokhina E, Wilson V, Goodship THJ, Perkins SJ. Osborne AJ, et al. Among authors: rallapalli pm. J Immunol. 2018 Apr 1;200(7):2464-2478. doi: 10.4049/jimmunol.1701695. Epub 2018 Mar 2. J Immunol. 2018. PMID: 29500241 Free PMC article.