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A family study of congenital dysfibrinogenemia caused by a novel mutation in the FGA gene: A case report
Congenital dysfibrinogenemia (CD) is a rare hereditary fibrinogen disorder characterized by normal fibrinogen antigen levels associated with lower functional activities. The aim of this study is to analyze the phenotype and genotype of a family of CD. Routine coagulation screening tests were perform...
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| Udgivet i: | Open Med (Wars) |
|---|---|
| Main Authors: | , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
De Gruyter
2020
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7712284/ https://ncbi.nlm.nih.gov/pubmed/33336034 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1515/med-2020-0214 |
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