– Genetic Drivers of Kidney Defects in the DiGeorge Syndrome
– EXTL3 mutations cause skeletal dysplasia, immune deficiency, and developmental delay
– Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease
– A missense variant in NCF1 is associated with susceptibility to multiple autoimmune diseases
– Genome-wide analysis of blood gene expression in migraine implicates immune-inflammatory pathways
Estudios genómicos aportan conocimientos sobre inmunidad
En la sección: Actualidades, Autoinmunidad, Inflamación, Tecnologías. Publicado en: . 
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