Fátima Sánchez Cabo

Learn More
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 great clinical variability and low genotype/phenotype(More)
Microarray technology is becoming an essential tool in functional genomics. The possibility of monitoring the expression level of thousands of genes simultaneously, as the response to a particular biological condition, gives to the biologists the chance to widen the aims of their experiments and opens a door to the understanding of cellular transcription(More)
  • 1