Three cases of congenital dysfibrinogenemia in unrelated Chinese families: heterozygous missense mutation in fibrinogen alpha chain Argl6His

Congenital dysfibrinogenemia (CD) is a qualitative fibrinogen disorder caused by an abnormal fibrinogen molecule structure, leading to dysfunctional blood coagulation. This study describes 3 cases of dysfibrinogenemia identified in the unrelated Chinese pedigrees. Routine coagulation screening tests...

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Shranjeno v:
Bibliografske podrobnosti
izdano v:Medicine (Baltimore)
Main Authors: Luo, Meiling, Deng, Donghong, Xiang, Liqun, Cheng, Peng, Liao, Lin, Deng, Xuelian, Yan, Jie, Lin, Faquan
Format: Artigo
Jezik:Inglês
Izdano: Wolters Kluwer Health 2016
Teme:
4800
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC5265910/
https://ncbi.nlm.nih.gov/pubmed/27684817
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MD.0000000000004864
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