Topologically equivalent mutations causing dysfunctional coagulation factors VII (294Ala→Val) and X (334Ser→ Pro)-Reference-Cited by-同舟云学术

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Topologically equivalent mutations causing dysfunctional coagulation factors VII (294Ala→Val) and X (334Ser→ Pro)

Published:1994 Issue:7 Volume:3 Page:1175-1177
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Hum Mol Genet

Author:

Bernardi F.,Castaman G.,Redaelll R.,Pinotti M.,Lunghl B.,Rodeghlero F.,Marchetti G.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/3/7/1175/2446731/3-7-1175.pdf

Cited by 31 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. A novel compound heterozygous variant linked to hematuria in a family with hereditary factor VII deficiency;The Journal of Gene Medicine;2021-12-30

2. Whole exome sequencing in the diagnostic workup of patients with a bleeding diathesis;Haemophilia;2018-11-15

3. Diagnostic single gene analyses beyond Sanger;Hämostaseologie;2017-07-17

4. The F7 Gene and Clotting Factor VII Levels: Dissection of a Human Quantitative Trait Locus;Human Biology;2009-12

5. Unexplained Discrepancies in the Activity—Antigen Ratio in Congenital FX Deficiencies With Defects in the Catalytic Domain;Clinical and Applied Thrombosis/Hemostasis;2009-08-09

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