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List of works by Pavithra M Rallapalli

An interactive mutation database for human coagulation factor IX provides novel insights into the phenotypes and genetics of hemophilia B ⬇️

scientific article published on July 1, 2013

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

scientific article published on 2 March 2018

The EAHAD Blood Coagulation Factor VII Variant Database

scientific article published on 25 April 2020

The European Association for Haemophilia and Allied Disorders (EAHAD) Coagulation Factor Variant Databases: Important resources for haemostasis clinicians and researchers

scientific article published on 13 March 2020

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