Human Fibrinogen: Molecular and Genetic Aspects of Congenital Disorders

Human Fibrinogen: Molecular and Genetic Aspects of Congenital Disorders

Congenital fibrinogen disorders can be quantitative (afibrinogenemia, hypofibrinogenemia) or functional (dysfibrinognemia). To date, several genetic variants have been identified in individuals with fibrinogen disorders. The complexity of the fibrinogen molecules, formed by three non-identical chain...

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Bibliographic Details
Main Authors: Giovanni Luca Tiscia, Maurizio Margaglione
Format: Article
Language:English
Published: MDPI AG 2018-05-01
Series:International Journal of Molecular Sciences
Subjects:
afibrinogenemia
hypofibrinogenemia
dysfibrinogenemia
Online Access:http://www.mdpi.com/1422-0067/19/6/1597

Internet

http://www.mdpi.com/1422-0067/19/6/1597

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