Complement component C7 deficiency in a Spanish family

Different genetic mutations have been described in complement component C7 deficiency, a molecular defect which is clinically associated with an increased susceptibility to neisserial recurrent infections, although some cases remain asymptomatic. In this work we report the genetic bases of C7 defici...

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Detalhes bibliográficos
Main Authors: VÁZQUEZ-BERMÚDEZ, M F, BARROSO, S, WALTER, K, ÁLVAREZ, A J, ALARCÓN, A, LÓPEZ-TRASCASA, M, WICHMANN, I, AGUILAR, F, NÚÑEZ-ROLDáN, A, SÁNCHEZ, B
Formato: Artigo
Idioma:Inglês
Publicado em: Blackwell Science Inc 2003
Assuntos:
Clinical Studies
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1808760/
https://ncbi.nlm.nih.gov/pubmed/12869030
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1046/j.1365-2249.2003.02186.x
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