Fibrinogen Columbus II: A novel c.1075G>T mutation in the FGG gene causing hypodysfibrinogenemia and thrombosis in an adolescent male-Reference-Cited by-同舟云学术

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Fibrinogen Columbus II: A novel c.1075G>T mutation in the FGG gene causing hypodysfibrinogenemia and thrombosis in an adolescent male

Published:2019-05-27 Issue:9 Volume:66 Page:
ISSN:1545-5009
Container-title:Pediatric Blood & Cancer
language:en
Short-container-title:Pediatr Blood Cancer

Author:

Kumar Riten¹²^ORCID,Dawson Jennifer³,Varga Elizabeth¹⁴,Canini Joan T.¹,Monda Kay L.¹,Dunn Amy L.¹²

Affiliation:

1. Division of Pediatric Hematology/Oncology/BMTNationwide Children's Hospital Columbus Ohio

2. Department of PediatricsThe Ohio State University Columbus Ohio

3. Department of Structural BiologySt. Jude Children's Research Hospital Memphis Tennessee

4. The Institute for Genomic MedicineNationwide Children's Hospital Columbus Ohio

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pbc.27832

Reference10 articles.

1. Genetics, diagnosis and clinical features of congenital hypodysfibrinogenemia: a systematic literature review and report of a novel mutation

2. Dysfibrinogenemia: from molecular anomalies to clinical manifestations and management

3. Diagnosis, clinical features and molecular assessment of the dysfibrinogenaemias

4. Treatment, Survival, and Thromboembolic Outcomes of Thrombotic Storm in Children

5. Crystal structure of a 30 kDa C-terminal fragment from the γ chain of human fibrinogen

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Mutations Accounting for Congenital Fibrinogen Disorders: An Update;Seminars in Thrombosis and Hemostasis;2022-01-24

2. Novel variant fibrinogen γp.C352R produced hypodysfibrinogenemia leading to a bleeding episode and failure of infertility treatment;International Journal of Hematology;2021-06-12

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