A rare mutation in the F12 gene in a patient with ... - BV FAPESP
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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

A rare mutation in the F12 gene in a patient with ACE inhibitor-induced angioedema

Full text
Author(s):
Veronez, Camila Lopes ; Serpa, Faradiba Sarquis ; Pesquero, Joao Bosco
Total Authors: 3
Document type: Letter
Source: ANNALS OF ALLERGY ASTHMA & IMMUNOLOGY; v. 118, n. 6, p. 743-745, JUN 2017.
Web of Science Citations: 3
Abstract

FAPESP's process: 13/02661-4 - Genetics of hereditary angioedema
Grantee:João Bosco Pesquero
Support Opportunities: Regular Research Grants
FAPESP's process: 11/24142-3 - Plasma Kallikrein Role in Hereditary Angioedema: Genetics and Functional Analysis.
Grantee:Camila Lopes Veronez
Support Opportunities: Scholarships in Brazil - Doctorate