Frequent genomic alteration is identified in a rare subset of breast cancer

22 abril 2015

Genomic profiling identifies genomic mutations in a gene associated with a rare subset of breast cancer, research shows — mutations that cannot otherwise be identified with standard clinical analysis of cells and tissue. The findings could have therapeutic implications specific to this rare form of the disease, say the authors.
http://feeds.sciencedaily.com/~r/sciencedaily/~3/bp1DD4FwWww/150422084048.htm

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