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A novel fibrinogen variant in a Chinese pedigree with congenital dysfibrinogenemia caused by FGA P. Arg38Thr mutation: A case report
RATIONALE: Congenital dysfibrinogenemia (CD) is characterized by altered functional properties of the fibrinogen; people who suffer from CD often have a low activity of fibrinogen and the mutation in the genomic DNA. PATIENT CONCERNS: A 6-year-old child was examined with a low activity of fibrinogen...
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| Publicado no: | Medicine (Baltimore) |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Wolters Kluwer Health
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6200480/ https://ncbi.nlm.nih.gov/pubmed/30290666 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MD.0000000000012697 |
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