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Phenotype and genotype comparisons in carriers of haemophilia A.

作者信息

Olsson A, Ljung R, Hellgren M, Berntorp E, Baghaei F

机构信息

Department of Haematology and Coagulation Disorders, Sahlgrenska University Hospital, Gothenburg, Sweden.

Department of Paediatrics, Centre for Thrombosis and Haemostasis, Skåne University Hospital, Lund University, Malmö, Sweden.

出版信息

Haemophilia. 2016 May;22(3):e235-7. doi: 10.1111/hae.12928. Epub 2016 Apr 4.

DOI:10.1111/hae.12928
PMID:27040322
Abstract
摘要

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引用本文的文献

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Women and girls with haemophilia receiving care at specialized haemophilia treatment centres in the United States.在美国专门的血友病治疗中心接受治疗的患血友病的妇女和女孩。
Haemophilia. 2021 Nov;27(6):1037-1044. doi: 10.1111/hae.14403. Epub 2021 Sep 4.
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Mutation analysis in the F8 gene in 485 families with haemophilia A and prenatal diagnosis in China.在中国,对 485 个血友病 A 家系 F8 基因的突变分析及产前诊断。
Haemophilia. 2021 Jan;27(1):e88-e92. doi: 10.1111/hae.14206. Epub 2020 Nov 27.
3
A decreased and less sustained desmopressin response in hemophilia A carriers contributes to bleeding.
血友病 A 携带者的去氨加压素反应减弱且持续时间更短,这有助于出血。
Blood Adv. 2018 Oct 23;2(20):2629-2636. doi: 10.1182/bloodadvances.2018023713.