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Genetic Study of Hereditary Angioedema Type I and Type II (First Report from Iranian Patients: Describing Three New Mutations)

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Year: 2020
Type: article
Study design: Observational Study
Source: Immunological Investigations
DOI: 10.1080/08820139.2020.1817068
Authors: Susan Nabilou, Fatemeh Pak, Zahra Alizadeh, Mohammad Reza Fazlollahi, Masoud Houshmand, Maryam Ayazi, Iraj Mohammadzadeh, Mohammad Hasan Bemanian, Abbas Fayezi, Mohammad Nabavi, Shiva Saghafi, Sajedeh Mohammadian, Parviz Kokhaei, Mostafa Moin, Zahra Pourpak
Institutions: Semnan University of Medical Sciences, Karolinska Institutet, Iran University of Medical Sciences, Tehran University of Medical Sciences, National Institute of Genetic Engineering and Biotechnology, Babol University of Medical Sciences, Rasool Akram Hospital, Ahvaz Jundishapur University of Medical Sciences
Language: English

Topic: Coagulation, Bradykinin, Polyphosphates, and Angioedema
Subfield: Hematology
Field: Medicine
Domain: Health Sciences
SDG: Good health and well-being

Open Access status: closed

Funders: Tehran University of Medical Sciences and Health Services, Semnan University of Medical Sciences and Health Services
OpenAlex ID: W3084032730
FWCI: 0.491
Cites: 28
Cited by: 3
Related to: 10
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