Fortuitous Discovery of Asymptomatic Homozygous Antithrombin Deficiency: A Rare p.Leu131Phe Heparin-Binding Site Mutation: A Case Report.

Cherkaoui S, Dedeken L, Demulder A, Simar J, Orlando C, Rozen L

DOI: 10.1002/jha2.70398
Published: 2026 Dec
Container: EJHaem
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.1002/jha2.70398,
  title = {Fortuitous Discovery of Asymptomatic Homozygous Antithrombin Deficiency: A Rare p.Leu131Phe Heparin-Binding Site Mutation: A Case Report.},
  author = {Cherkaoui S and Dedeken L and Demulder A and Simar J and Orlando C and Rozen L},
  year = {2026},
  journal = {EJHaem},
  doi = {10.1002/jha2.70398},
  url = {https://doi.org/10.1002/jha2.70398}
}

RIS

TY  - JOUR
TI  - Fortuitous Discovery of Asymptomatic Homozygous Antithrombin Deficiency: A Rare p.Leu131Phe Heparin-Binding Site Mutation: A Case Report.
AU  - Cherkaoui S
AU  - Dedeken L
AU  - Demulder A
AU  - Simar J
AU  - Orlando C
AU  - Rozen L
PY  - 2026
JO  - EJHaem
DO  - 10.1002/jha2.70398
UR  - https://doi.org/10.1002/jha2.70398
ER  -

APA

S, C., L, D., A, D., J, S., C, O., & L, R. (2026). Fortuitous Discovery of Asymptomatic Homozygous Antithrombin Deficiency: A Rare p.Leu131Phe Heparin-Binding Site Mutation: A Case Report.. EJHaem. https://doi.org/10.1002/jha2.70398

Source records

pubmed · retrieved 2026-11-10T06:50:32.830Z