Genetic variants at the chromosomal region 2q21.3 underlying inhibitor development in patients with severe haemophilia A

INTRODUCTION: Inhibitor development affects about 30% of patients with severe haemophilia A (HA) and results from different environmental and genetic risk factors. Previously, we identified the missense variant rs3754689 in the LCT gene linked with this predisposition. Since rs3754689 variant is ben...

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Detalles Bibliográficos
Autores principales: Spena, Silvia, Cairo, Andrea, Pappalardo, Emanuela, Gorski, Marcin M., Garagiola, Isabella, Hassan, Shermarke, Gualtierotti, Roberta, Peyvandi, Flora
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9306754/
https://www.ncbi.nlm.nih.gov/pubmed/35182444
http://dx.doi.org/10.1111/hae.14503

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9306754/
https://www.ncbi.nlm.nih.gov/pubmed/35182444
http://dx.doi.org/10.1111/hae.14503

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