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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Detalles Bibliográficos
Autores principales: Luo, Meiling, Deng, Donghong, Xiang, Liqun, Cheng, Peng, Liao, Lin, Deng, Xuelian, Yan, Jie, Lin, Faquan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2016
Materias:
4800
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5265910/
https://www.ncbi.nlm.nih.gov/pubmed/27684817
http://dx.doi.org/10.1097/MD.0000000000004864

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5265910/
https://www.ncbi.nlm.nih.gov/pubmed/27684817
http://dx.doi.org/10.1097/MD.0000000000004864

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