A myoferlin gain‐of‐function variant associates with a new type of hereditary angioedema
Copyright policy ) Anastasia Ariano; Maria D'Apolito; Maria Bova; Francesco Bellanti; Stefania Loffredo; Giovanna D'Andrea; Mariano Intrieri; +5 Authors
Anastasia Ariano; Maria D'Apolito; Maria Bova; Francesco Bellanti; Stefania Loffredo; Giovanna D'Andrea; Mariano Intrieri; Angelica Petraroli; Angela Bruna Maffione; Giuseppe Spadaro; Rosa Santacroce; Maurizio Margaglione;
A myoferlin gain‐of‐function variant associates with a new type of hereditary angioedema
Italy
- National Research Council Italy
- University Federico II of Naples Italy
- National Academies of Sciences, Engineering, and Medicine United States
- University of Molise Italy
- University of Foggia Italy
angioedema; basic mechanisms; genetics, angioedema, Gain of Function Mutation, Angioedemas, Hereditary, Humans, genetics, basic mechanisms, basic mechanism, Complement C1 Inactivator Proteins, Complement C1 Inhibitor Protein
angioedema; basic mechanisms; genetics, angioedema, Gain of Function Mutation, Angioedemas, Hereditary, Humans, genetics, basic mechanisms, basic mechanism, Complement C1 Inactivator Proteins, Complement C1 Inhibitor Protein
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This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
Citations provided by BIP!popularityPopularity provided by BIP!
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
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