Clinical Validation of an Automated Fluorogenic Factor XIII Activity Assay Based on Isopeptidase Activity

Hereditary factor XIII (FXIII) deficiency is a rare autosomal bleeding disorder which can cause life-threatening bleeding. Acquired deficiency can be immune-mediated or due to increased consumption or reduced synthesis. The most commonly used screening test is insensitive, and widely used quantitati...

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Detalles Bibliográficos
Autores principales: Leitner, Martina, Büchold, Christian, Pasternack, Ralf, Binder, Nikolaus B., Moore, Gary W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7863959/
https://www.ncbi.nlm.nih.gov/pubmed/33498248
http://dx.doi.org/10.3390/ijms22031002

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7863959/
https://www.ncbi.nlm.nih.gov/pubmed/33498248
http://dx.doi.org/10.3390/ijms22031002

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