Publication | Open Access
Severe thrombophilia in a factor V‐deficient patient homozygous for the Ala2086Asp mutation (FV Besançon)
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Citations
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References
2021
Year
ThrombosisGenetic DisorderImmunodeficienciesHematologyImmunologyPathologyAla2086asp MutationFv BesançonMedical GeneticsMedicineSevere ThrombophiliaInborn Error Of Immunity
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