Hereditary Angioedema Due to C1 Inhibitor Deficiency in Serbia: Two Novel Mutations and Evidence of Genotype-Phenotype Association

Open Access

Peer-reviewed

Research Article

Slađana Andrejević,

Affiliation Clinic of Allergology and Immunology, Clinical Center of Serbia, Belgrade, Serbia
⨯
Peter Korošec,

Affiliation University Clinic of Respiratory and Allergic Diseases Golnik, Golnik, Slovenia
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Mira Šilar,

Affiliation University Clinic of Respiratory and Allergic Diseases Golnik, Golnik, Slovenia
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Mitja Košnik,

Affiliation University Clinic of Respiratory and Allergic Diseases Golnik, Golnik, Slovenia
⨯
Radovan Mijanović,

Affiliation Clinic of Allergology and Immunology, Clinical Center of Serbia, Belgrade, Serbia
⨯
Branka Bonači-Nikolić,

Affiliation Clinic of Allergology and Immunology, Clinical Center of Serbia, Belgrade, Serbia
⨯
Matija Rijavec

* E-mail: matija.rijavec@klinika-golnik.si

Affiliation University Clinic of Respiratory and Allergic Diseases Golnik, Golnik, Slovenia
⨯

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Frameshift mutation
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Nonsense mutation
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Edema
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Deletion mutation
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Mutation detection
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Insertion mutation
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Missense mutation
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Substitution mutation
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