Factor X heterozygous mutation in a patient with potential risk of bleeding: A case report

RATIONALE: Factor X (FX) deficiency is a rare autosomal recessive bleeding disorder. The majority of patients carry a missense mutation in F10, and patients with bleeding disorders are either homozygous or compound heterozygous for F10. Nonsense mutations are exceptionally rare, and a heterozygous n...

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Detalles Bibliográficos
Autores principales: Arita, Kotaro, Niimi, Hideki, Yamagishi, Nana, Ueno, Tomohiro, Kitajima, Isao, Sugiyama, Toshiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5999474/
https://www.ncbi.nlm.nih.gov/pubmed/29879041
http://dx.doi.org/10.1097/MD.0000000000010950

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5999474/
https://www.ncbi.nlm.nih.gov/pubmed/29879041
http://dx.doi.org/10.1097/MD.0000000000010950

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