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pro vyhledávání: '"Victor Koji Nakamura"'
Autor:
Christiane Stieber, Nathália Cagini, L. Karla Arruda, Sven Cichon, Victor Koji Nakamura, Eliana de Toledo, Fabio Fernandes Morato Castro, Solange Rodrigues Valle, Miguel Alberto Piccirillo, Faradiba Sarquis Serpa, Anete Sevciovic Grumach, João Bosco Pesquero, Gabriela Andrade Coelho Dias, Rosemeire Navickas Constantino-Silva, M. Bernardes, Mariana Paes Leme Ferriani, Camila Lopes Veronez, Eli Mansour, Rozana Fátima Gonçalves, Adriana S. Moreno, Luana S.M. Maia
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
Background Hereditary angioedema (HAE) with normal C1 inhibitor (C1-INH) is a rare condition with clinical features similar to those of HAE with C1-INH deficiency. Mutations in the F12 gene have been identified in subsets of patients with HAE with no
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ad63368dc71480b2d6bf8ca058c0306
