Disease-modifying factors in hereditary angioedema: an RNA expression-based screening

BACKGROUND: Hereditary Angioedema due to C1-Inhibitor deficiency (HAE types I and II) is a monogenic disease characterized by sudden, self-limited episodes of cutaneous and mucosal swelling due to local deregulation of vascular permeability. Despite its monogenic pattern of inheritance, HAE exhibits...

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Detalles Bibliográficos
Autores principales: López-Lera, Alberto, Cabo, Fátima Sánchez, Garrido, Sofía, Dopazo, Ana, López-Trascasa, Margarita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3671971/
https://www.ncbi.nlm.nih.gov/pubmed/23688356
http://dx.doi.org/10.1186/1750-1172-8-77

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3671971/
https://www.ncbi.nlm.nih.gov/pubmed/23688356
http://dx.doi.org/10.1186/1750-1172-8-77

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