Targeted long-read sequencing identifies a novel 1.3 kb FGG deletion associated with variable bleeding and thrombotic phenotypes in hypofibrinogenemia
- DOI
- 10.1016/j.rpth.2026.107001
- Published
- 2026-10
- Container
- Research and Practice in Thrombosis and Haemostasis
- Publisher
- Elsevier BV
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1016/j.rpth.2026.107001,
title = {Targeted long-read sequencing identifies a novel 1.3 kb FGG deletion associated with variable bleeding and thrombotic phenotypes in hypofibrinogenemia},
author = {Alexander Couzens and Frédéric Masclaux and Baptiste Micheli and Michel Guipponi and Alexandre Butelet and Colette Ballan-Legin and Alessandro Casini and Marguerite Neerman-Arbez},
year = {2026},
journal = {Research and Practice in Thrombosis and Haemostasis},
doi = {10.1016/j.rpth.2026.107001},
url = {https://doi.org/10.1016/j.rpth.2026.107001}
}RIS
TY - JOUR TI - Targeted long-read sequencing identifies a novel 1.3 kb FGG deletion associated with variable bleeding and thrombotic phenotypes in hypofibrinogenemia AU - Alexander Couzens AU - Frédéric Masclaux AU - Baptiste Micheli AU - Michel Guipponi AU - Alexandre Butelet AU - Colette Ballan-Legin AU - Alessandro Casini AU - Marguerite Neerman-Arbez PY - 2026 JO - Research and Practice in Thrombosis and Haemostasis DO - 10.1016/j.rpth.2026.107001 UR - https://doi.org/10.1016/j.rpth.2026.107001 ER -
APA
Couzens, A., Masclaux, F., Micheli, B., Guipponi, M., Butelet, A., Ballan-Legin, C., Casini, A., & Neerman-Arbez, M. (2026). Targeted long-read sequencing identifies a novel 1.3 kb FGG deletion associated with variable bleeding and thrombotic phenotypes in hypofibrinogenemia. Research and Practice in Thrombosis and Haemostasis. https://doi.org/10.1016/j.rpth.2026.107001
Source records
- crossref · retrieved 2026-11-10T12:40:23.308Z