Genetic Variation of Kallikrein-Kinin System and Related Genes in Patients With Hereditary Angioedema

Hereditary angioedema (HAE) is an autosomal dominant disease caused by C1-INH deficiency due to mutations in SERPING1 (C1-INH-HAE) in most of the cases, or by specific mutations in factor XII gene, F12 (F12-HAE). Identification of polymorphisms in the genes encoding proteins from key pathways drivin...

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Detalles Bibliográficos
Autores principales: Veronez, Camila Lopes, Aabom, Anne, Martin, Renan Paulo, Filippelli-Silva, Rafael, Gonçalves, Rozana Fátima, Nicolicht, Priscila, Mendes, Agatha Ribeiro, Da Silva, Jane, Guilarte, Mar, Grumach, Anete Sevciovic, Mansour, Eli, Bygum, Anette, Pesquero, João Bosco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6393376/
https://www.ncbi.nlm.nih.gov/pubmed/30847342
http://dx.doi.org/10.3389/fmed.2019.00028

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6393376/
https://www.ncbi.nlm.nih.gov/pubmed/30847342
http://dx.doi.org/10.3389/fmed.2019.00028

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