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Dysfibrinogenaemia associated with a novel heterozygous mutation in FGB (c.680delG) and a mild clinical history of bleeding.

By A. Priovolos, M. Neerman-Arbez, M. Morris, A. Angelillo-Scherrer and J. Nötzli
Publisher: 'Ovid Technologies (Wolters Kluwer Health)'
Year: 2015
DOI identifier: 10.1097/MBC.0000000000000196
OAI identifier: oai:serval.unil.ch:BIB_822D5551B04F
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