Protein modelling to understand FGB mutations leading to congenital hypofibrinogenaemia.

Alessandro CasiniR VilarY BeauverdD AslanK DevreeseV MondelaersL AlberioC GubertP de MoerlooseM Neerman-Arbez

Published in: Haemophilia : the official journal of the World Federation of Hemophilia (2017)

Protein modelling of new causative mutations and comparison of molecular, biochemical and clinical data continue to yield valuable information on the development and course of fibrinogen disorders as well as on the choice of the most appropriate treatments.

Keyphrases

protein protein
amino acid
binding protein
electronic health record
healthcare
big data
single molecule
small molecule
deep learning
data analysis