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Molecular characterization of iranian patients with inherited coagulation factor VII deficiency Cover

Molecular characterization of iranian patients with inherited coagulation factor VII deficiency

Balkan Journal of Medical Genetics
Volume 20 (2017): Issue 2 (December 2017)
By: S Shahbazi,  R Mahdian,  K Karimi and  A Mashayekhi  
Open Access
|Dec 2017

Authors

S Shahbazi

sh.shahbazi@modares.ac.ir

Department of Medical Genetics, Faculty of Medical Sciences, Tarbiat Modares University Tehran, Tehran, Iran

R Mahdian

Molecular Medicine Department, Pasteur Institute of Iran, Tehran, Iran

K Karimi

Clinic of Hematology and Oncology, School of Medical Sciences, Tehran University of Medical Sciences, Tehran, Iran

A Mashayekhi

Department of Medical Genetics, Faculty of Medical Sciences, Tarbiat Modares University Tehran, Tehran, Iran
DOI: https://doi.org/10.1515/bjmg-2017-0027 | Journal eISSN: 2199-5761
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Language: English
Page range: 19 - 25
Published on: Dec 29, 2017
Published by: Macedonian Academy of Sciences and Arts
In partnership with: Paradigm Publishing Services
Publication frequency: 2 issues per year
Keywords:
Coagulation factor VII (FVII) deficiency,
F7 gene,
mRNA sequencing,
Mutation detection
Related subjects:
Medicine,
Basic medical science,
Basic medical science, other

© 2017 S Shahbazi, R Mahdian, K Karimi, A Mashayekhi, published by Macedonian Academy of Sciences and Arts
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

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