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Statistical Validation of Rare Complement Variants Provides Insights into the Molecular Basis of Atypical Hemolytic Uremic Syndrome and C3 Glomerulopathy.

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Description scientific article published on 2 March 2018
Author/s

author: Daniel P Gale  Nicolo Ghiringhelli Borsa  David Kavanagh  Pavithra M Rallapalli  Stephen J Perkins  Marina Noris  Amy J Osborne  Paula Vieira-Martins  Véronique Frémeaux-Bacchi  Santiago Rodriguez de Córdoba  Giuseppe Remuzzi  Richard J Smith  Timothy H J Goodship 

Publication date March 2, 2018
Language English
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