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Mutational spectrum and genotype-phenotype relationships in a cohort of Romanian hereditary angioedema patients caused by C1 inhibitor deficiency Cover

Mutational spectrum and genotype-phenotype relationships in a cohort of Romanian hereditary angioedema patients caused by C1 inhibitor deficiency

Revista Romana de Medicina de Laborator
Volume 27 (2019): Issue 3 (July 2019)
By: Gabriella Gábos,  Dumitru Moldovan,  Daniela Dobru,  Enikő Mihály,  Noémi Bara,  Valentin Nădășan,  Adina Hutanu and  Katalin Csép  
Open Access
|Jul 2019
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DOI: https://doi.org/10.2478/rrlm-2019-0029 | Journal eISSN: 2284-5623 | Journal ISSN: 1841-6624
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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:
hereditary angioedema,
C1 inhibitor deficiency,
SERPING1
Related subjects:
Life sciences,
Molecular biology,
Biochemistry,
Human biology,
Microbiology and virology

© 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.

Volume 27 (2019): Issue 3 (July 2019)
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