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Prothrombin Gene Mutation as a Teaching Tool: An Autobiographical Case Report
The prothrombin G20210A factor II mutation carrier status has been reported to cause complications during pregnancy. This report presents the case of a patient diagnosed with heterozygous prothrombin G20210A factor II mutation at 29 years of age during preconception genetic screening. The patient ha...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9938718/ https://www.ncbi.nlm.nih.gov/pubmed/36820119 http://dx.doi.org/10.7759/cureus.33967 |