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Complement component C7 deficiency in two Spanish families

Different genetic mutations have been described in complement component C7 deficiency, a molecular defect clinically associated with an increased susceptibility to neisserial recurrent infections. In this work we report the genetic basis of C7 deficiency in two different Spanish families (family 1 a...

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Detalhes bibliográficos
Main Authors: Barroso, Sonia, Sánchez, Berta, Álvarez, Antonia José, López-Trascasa, Margarita, Lanuza, Amparo, Luque, Rafael, Wichmann, Ingeborg, Núñez-Roldán, Antonio
Formato: Artigo
Idioma:Inglês
Publicado em: Blackwell Science Inc 2004
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1782596/
https://ncbi.nlm.nih.gov/pubmed/15554930
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1365-2567.2004.01997.x
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