Spectrum of mutations in Indian patients with fibrinogen disorders and its application in genetic diagnosis of the affected families-Reference-Cited by-同舟云学术

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Spectrum of mutations in Indian patients with fibrinogen disorders and its application in genetic diagnosis of the affected families

Published:2015-08-17 Issue:6 Volume:21 Page:e519-e523
ISSN:1351-8216
Container-title:Haemophilia
language:en
Short-container-title:Haemophilia

Author:

Mukaddam A.¹,Kulkarni B.¹,Jadli A.¹,Ghosh K.¹,Shetty S.¹

Affiliation:

1. National Institute of Immunohaematology (ICMR); KEM Hospital; Parel Mumbai India

Funder

Indian Council of Medical Research

Publisher

Wiley

Subject

Genetics (clinical),Hematology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/hae.12788/fullpdf

Cited by 5 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. Homeopathic Management of Afibrinogenemia along with Beta-Thalassemia;AYUHOM;2022

3. Analysis of an Inherited Dysfibrinogenemia Pedigree Associated with a Heterozygous Mutation in the FGA Gene;Hämostaseologie;2020-12

4. A genetic modifier of venous thrombosis in zebrafish reveals a functional role for fibrinogen AαE in early hemostasis;Blood Advances;2020-11-09

5. Identification of Two Novel Fibrinogen Bβ Chain Mutations in Two Slovak Families with Quantitative Fibrinogen Disorders;International Journal of Molecular Sciences;2017-12-29

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