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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...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
De Gruyter
2020
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7712284/ https://www.ncbi.nlm.nih.gov/pubmed/33336034 http://dx.doi.org/10.1515/med-2020-0214 |