Genetics, diagnosis and clinical features of congenital hypodysfibrinogenemia: a systematic literature review and report of a novel mutation
A. Casini; T. Brungs; C. Lavenu‐Bombled; R. Vilar; M. Neerman‐Arbez; P. de Moerloose
Author Information: Division of Angiology and Haemostasis
|Checking for direct PDF access through Ovid|
Abstract unavailable for this article.