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A Novel Phenotype of the Factor 5 Gene Mutation (Homozygote Met1736Val and Heterozygote Asp68His) Is Associated With Moderate Factor V Deficiency
BACKGROUND: Factor V (FV) deficiency is a rare disease, with a low incidence rate in Asia. Therefore, the F5 mutation in the Taiwanese population is poorly understood. METHODS: A Chinese family with FV deficiency was included, and the patient and his family members underwent mutation analysis. Then,...
| Autores principales: | , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Frontiers Media S.A.
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9219604/ https://www.ncbi.nlm.nih.gov/pubmed/35755047 http://dx.doi.org/10.3389/fmed.2022.870269 |