Heterozygosity in factor XIII genes and the manifestation of mild inherited factor XIII deficiency.

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作者： Sneha,Singh ^[1] ; Behnaz,Pezeshkpoor ^[1] ; Muhammad Ahmer,Jamil ^[1] ; Johannes,Dodt ^[2] ; Amit,Sharma ^[3] ; Vasanth,Ramar ^[1] ; Vytautas,Ivaskevicius ^[1] ; Emma,Hethershaw ^[4] ; Helen,Philippou ^[4] ; Anna,Pavlova ^[1] ; Johannes,Oldenburg ^[1] ; Arijit,Biswas ^[5]

作者单位： Institute for Experimental Hematology and Transfusion Medicine, University Hospital of Bonn, Bonn, North-Rheine Westfalen, Germany. ^[1] Paul-Ehrlich Institute, Langen, Hessen, Germany. ^[2] Department of Hematology, All India Institute of Medical Sciences, New Delhi, India. ^[3] Division of Cardiovascular and Diabetes Research, School of Medicine, University of Leeds, Leeds, United Kingdom. ^[4] Institute for Experimental Hematology and Transfusion Medicine, University Hospital of Bonn, Bonn, North-Rheine Westfalen, Germany. Electronic address: arijit.biswas@ukbonn.de. ^[5]

关键词 factor XIII factor XIII deficiency fibrinogen missense mutations next-generation sequencing

主题词人类(Humans);因子ⅩⅢ(Factor XIII);因子ⅩⅢ缺乏(Factor XIII Deficiency);纤维蛋白原(Fibrinogen);出血(Hemorrhage);止血药(Hemostatics);回顾性研究(Retrospective Studies)

DOI 10.1016/j.jtha.2023.09.032

PMID 37832789

发布时间 2024-02-07

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