Factor VII deficiency: Unveiling the cellular and molecular mechanisms underlying three model alterations of the enzyme catalytic domain-Reference-Cited by-同舟云学术

Factor VII deficiency: Unveiling the cellular and molecular mechanisms underlying three model alterations of the enzyme catalytic domain

Published:2018-03 Issue:3 Volume:1864 Page:660-667
ISSN:0925-4439
Container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
language:en
Short-container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease

Author:

Chollet Maria Eugenia,Andersen Elisabeth,Skarpen Ellen,Myklebust Christiane F.,Koehler Christian,Morth Jens Preben,Chuansumrit Ampaiwan,Pinotti Mirko,Bernardi Francesco,Thiede Bernd,Sandset Per Morten,Skretting Grethe

Publisher

Elsevier BV

Subject

Molecular Biology,Molecular Medicine

Reference31 articles.

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2. Deficiency;Perry;Br. J. Haematol.,2002

3. Factor VII deficiency;Mariani;Semin. Thromb. Hemost.,2009

4. Rare bleeding disorders: diagnosis and treatment;Palla;Blood,2015

5. Factor VII deficiency and the FVII mutation database;Mcvey;Hum. Mutat.,2001

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3. Mutations of TFPI-binding exosites on factor VII cause bleeding phenotypes in factor VII deficiency;Blood Advances;2022-11-22

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

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