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Researchers develop a rapid blood test that diagnoses rare genetic diseases with 83% accuracy.
Researchers from the University of Melbourne have developed a new blood test that can rapidly diagnose thousands of rare genetic diseases by sequencing proteins instead of genes.
The test requires only a small blood sample and can differentiate between carriers and affected individuals.
With 83% accuracy, it identifies gene mutations linked to rare inherited diseases, potentially streamlining diagnosis and treatment.
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Los investigadores desarrollan una prueba de sangre rápida que diagnostica enfermedades genéticas raras con un 83% de precisión.