New Mutations in SERPING1, the Gene Coding for C1 Inhibitor, in Patients with Hereditary Angioedema in Brazil - 03/02/15
Doi : 10.1016/j.jaci.2014.12.1576
Adriana S. Moreno, PhD 1, 2, Luana Delcaro, BSc 1, Marina M. Dias, Chem 1, Solange R. Valle, MD, PhD 3, Alfeu T. França, MD 3, Soloni Levy, MD 3, Persio Roxo, MD, PhD 4, Wilson da Silva Junior 2, 5, Luisa Karla P. Arruda, MD, PhD, FAAAAI 1
1 Ribeirao Preto Medical School - University of Sao Paulo, Ribeirao Preto, Brazil
2 Center for Medical Genomics, Clinical Hospital of Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto, Brazil, Brazil
3 Clementino Fraga Filho University Hospital- UFRJ, Rio de Janeiro, Brazil
4 Department of Pediatrics, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto, Brazil, Brazil
5 Department of Genetics, School of Medicine of Ribeirao Preto - FMRP, Ribeirao Preto, Brazil
635
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© 2015
Publicado por Elsevier Masson SAS.
Vol 135 - N° 2S
P. AB196 - février 2015 Regresar al número
Artículo precedente
- Hereditary Angioedema Deaths: A Review from the Romanian Registry
- D. Moldovan, E. Mihály, N. Bara, V. N?d?san, Zs. Jeremiás
- Successful Management of Hereditary Angioedema (HAE) and Thrombophilia during Pregnancy: A Case Study
- Inmaculada Martinez-Saguer, Wolfhart Kreuz
Bienvenido a EM-consulte, la referencia de los profesionales de la salud.
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