As we enter the post genome era, the genes responsible for many different types of SCID have been identified and it is very likely that many more will follow. The challenge remains to use this information to expand our understanding of the pathogenesis of the disease and to continue to develop improved methods of diagnosis and treatment for affected individuals.
CITATION STYLE
Gaspar, H. B., Gilmour, K. C., & Jones, A. M. (2001). Severe combined immunodeficiency - Molecular pathogenesis and diagnosis. Archives of Disease in Childhood, 84(2), 169–173. https://doi.org/10.1136/adc.84.2.169
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