Fibrinogen Columbus III: A novel c.963del frameshift mutation in the FGG gene resulting in hypofibrinogenemia with a bleeding phenotype-Reference-Cited by-同舟云学术

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Fibrinogen Columbus III: A novel c.963del frameshift mutation in the FGG gene resulting in hypofibrinogenemia with a bleeding phenotype

Published:2020-10-15 Issue:3 Volume:68 Page:
ISSN:1545-5009
Container-title:Pediatric Blood & Cancer
language:en
Short-container-title:Pediatr Blood Cancer

Author:

Abdelghani Eman¹²^ORCID,Dawson Jennifer³,Zajo Kristin¹,Hallam Michelle¹,Dunn Amy¹²,Kumar Riten⁴⁵^ORCID

Affiliation:

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

2. Department of Pediatrics The Ohio State University Columbus Ohio

3. Genomic Medicine Lerner Research Institute Cleveland Clinic Cleveland Ohio

4. Dana‐Farber/Boston Children's Cancer and Blood Disorders Center Boston Massachusetts

5. Department of Pediatrics Harvard Medical School Boston Massachusetts

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pbc.28713

Reference12 articles.

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

2. Diagnosis and classification of congenital fibrinogen disorders: communication from the SSC of the ISTH

3. Mutational epidemiology of congenital fibrinogen disorders;Casini A;Thromb Haemost,2018

4. Fast, scalable generation of high‐quality protein multiple sequence alignments using Clustal Omega

5. Expression and analysis of a split premature termination codon in FGG responsible for congenital afibrinogenemia: escape from RNA surveillance mechanisms in transfected cells

Cited by 1 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

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