Mutational spectrum and genotype-phenotype relationships in a cohort of Romanian hereditary angioedema patients caused by C1 inhibitor deficiency
Authors
Gabriella Gábos
Lotus Life Clinic, Târgu Mureș, Romania
Romanian Network for Hereditary Angioedema, Romania
Dumitru Moldovan
Romanian Network for Hereditary Angioedema, Romania
Mures County Hospital Allergology-Immunology Department, Târgu Mureș, Romania
Daniela Dobru
University of Medicine, Pharmacy, Sciences and Technology of Târgu Mureș, Romania
Mures County Hospital Gastroenterology Department, Târgu Mureș, Romania
Enikő Mihály
Romanian Network for Hereditary Angioedema, Romania
Mures County Hospital Allergology-Immunology Department, Târgu Mureș, Romania
Noémi Bara
Romanian Network for Hereditary Angioedema, Romania
Valentin Nădășan
Romanian Network for Hereditary Angioedema, Romania
Department of Hygiene, University of Medicine, Pharmacy, Sciences and Technology of Târgu Mures, Romania
Adina Hutanu
Center for Advanced Medical and Pharmaceutical Research, University of Medicine, Pharmacy, Sciences and Technology of Târgu Mureș, Romania
Katalin Csép
Genetics Department, University of Medicine, Pharmacy, Sciences and Technology of Târgu Mureș, Romania
Language: English
Page range: 255 - 267
Submitted on: Feb 13, 2019
Accepted on: May 31, 2019
Published on: Jul 30, 2019
Published by: Romanian Association of Laboratory Medicine
In partnership with: Paradigm Publishing Services
Publication frequency: 4 issues per year
Keywords:
Related subjects:
© 2019 Gabriella Gábos, Dumitru Moldovan, Daniela Dobru, Enikő Mihály, Noémi Bara, Valentin Nădășan, Adina Hutanu, Katalin Csép, published by Romanian Association of Laboratory Medicine
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.