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Publications by Sheila Pinto
Complement Factor H Variants I890 and L1007 While Commonly Associated With Atypical Hemolytic Uremic Syndrome Are Polymorphisms With No Functional Significance
Kidney International
Nephrology
Statistical Validation of Rare Complement Variants Provides Insights Into the Molecular Basis of Atypical Hemolytic Uremic Syndrome and C3 Glomerulopathy
Journal of Immunology
Allergy
Immunology
Genetics of Atypical Hemolytic Uremic Syndrome (aHUS)
Seminars in Thrombosis and Hemostasis
Cardiovascular Medicine
Hematology
Cardiology
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